Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))

Isabelle Audo; Kinga Bujakowska; Elise Orhan; Charlotte M. Poloschek; Sabine Defoort-Dhellemmes; Isabelle Drumare; Susanne Kohl; Tien D. Luu; Odile Lecompte; Eberhart Zrenner; Marie Elise Lancelot; Aline Antonio; Aurore Germain; Christelle Michiels; Claire Audier; Mélanie Letexier; Jean Paul Saraiva; Bart P. Leroy; Francis L. Munier; Saddek Mohand-Saïd; Birgit Lorenz; Christoph Friedburg; Markus Preising; Ulrich Kellner; Agnes B. Renner; Veselina Moskova-Doumanova; Wolfgang Berger; Bernd Wissinger; Christian P. Hamel; Daniel F. Schorderet; Elfride De Baere; Dror Sharon; Eyal Banin; Samuel G. Jacobson; Dominique Bonneau; Xavier Zanlonghi; Guylene Le Meur; Ingele Casteels; Robert Koenekoop; Vernon W. Long; Francoise Meire; Katrina Prescott; Thomy De Ravel; Ian Simmons; Hoan Nguyen; Hélène Dollfus; Olivier Poch; Thierry Léveillard; Kim Nguyen-Ba-Charvet; José Alain Sahel; Shomi S. Bhattacharya; Christina Zeitz

doi:10.1016/j.ajhg.2012.06.001

Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))

Isabelle Audo
, Kinga Bujakowska
, Elise Orhan
, Charlotte M. Poloschek
, Sabine Defoort-Dhellemmes
, Isabelle Drumare
, Susanne Kohl
, Tien D. Luu
, Odile Lecompte
, Eberhart Zrenner
, Marie Elise Lancelot
, Aline Antonio
, Aurore Germain
, Christelle Michiels
, Claire Audier
, Mélanie Letexier
, Jean Paul Saraiva
, Bart P. Leroy
, Francis L. Munier
, Saddek Mohand-Saïd

Birgit Lorenz, Christoph Friedburg, Markus Preising, Ulrich Kellner, Agnes B. Renner, Veselina Moskova-Doumanova, Wolfgang Berger, Bernd Wissinger, Christian P. Hamel, Daniel F. Schorderet, Elfride De Baere, Dror Sharon, Eyal Banin, Samuel G. Jacobson, Dominique Bonneau, Xavier Zanlonghi, Guylene Le Meur, Ingele Casteels, Robert Koenekoop, Vernon W. Long, Francoise Meire, Katrina Prescott, Thomy De Ravel, Ian Simmons, Hoan Nguyen, Hélène Dollfus, Olivier Poch, Thierry Léveillard, Kim Nguyen-Ba-Charvet, José Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz^*

^*Corresponding author for this work

Institute for Medical Research Israel-Canada (IMRIC)

Research output: Contribution to journal › Comment/debate

Original language	English
Pages (from-to)	209
Number of pages	1
Journal	American Journal of Human Genetics
Volume	91
Issue number	1
DOIs	https://doi.org/10.1016/j.ajhg.2012.06.001
State	Published - 13 Jul 2012

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10.1016/j.ajhg.2012.06.001

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Audo, I., Bujakowska, K., Orhan, E., Poloschek, C. M., Defoort-Dhellemmes, S., Drumare, I., Kohl, S., Luu, T. D., Lecompte, O., Zrenner, E., Lancelot, M. E., Antonio, A., Germain, A., Michiels, C., Audier, C., Letexier, M., Saraiva, J. P., Leroy, B. P., Munier, F. L., ... Zeitz, C. (2012). Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330)). American Journal of Human Genetics, 91(1), 209. https://doi.org/10.1016/j.ajhg.2012.06.001

@article{179cf908dcce40b98736eeee4cc92b06,

title = "Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))",

author = "Isabelle Audo and Kinga Bujakowska and Elise Orhan and Poloschek, \{Charlotte M.\} and Sabine Defoort-Dhellemmes and Isabelle Drumare and Susanne Kohl and Luu, \{Tien D.\} and Odile Lecompte and Eberhart Zrenner and Lancelot, \{Marie Elise\} and Aline Antonio and Aurore Germain and Christelle Michiels and Claire Audier and M{\'e}lanie Letexier and Saraiva, \{Jean Paul\} and Leroy, \{Bart P.\} and Munier, \{Francis L.\} and Saddek Mohand-Sa{\"i}d and Birgit Lorenz and Christoph Friedburg and Markus Preising and Ulrich Kellner and Renner, \{Agnes B.\} and Veselina Moskova-Doumanova and Wolfgang Berger and Bernd Wissinger and Hamel, \{Christian P.\} and Schorderet, \{Daniel F.\} and \{De Baere\}, Elfride and Dror Sharon and Eyal Banin and Jacobson, \{Samuel G.\} and Dominique Bonneau and Xavier Zanlonghi and \{Le Meur\}, Guylene and Ingele Casteels and Robert Koenekoop and Long, \{Vernon W.\} and Francoise Meire and Katrina Prescott and \{De Ravel\}, Thomy and Ian Simmons and Hoan Nguyen and H{\'e}l{\`e}ne Dollfus and Olivier Poch and Thierry L{\'e}veillard and Kim Nguyen-Ba-Charvet and Sahel, \{Jos{\'e} Alain\} and Bhattacharya, \{Shomi S.\} and Christina Zeitz",

year = "2012",

month = jul,

day = "13",

doi = "10.1016/j.ajhg.2012.06.001",

language = "אנגלית",

volume = "91",

pages = "209",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

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Audo, I, Bujakowska, K, Orhan, E, Poloschek, CM, Defoort-Dhellemmes, S, Drumare, I, Kohl, S, Luu, TD, Lecompte, O, Zrenner, E, Lancelot, ME, Antonio, A, Germain, A, Michiels, C, Audier, C, Letexier, M, Saraiva, JP, Leroy, BP, Munier, FL, Mohand-Saïd, S, Lorenz, B, Friedburg, C, Preising, M, Kellner, U, Renner, AB, Moskova-Doumanova, V, Berger, W, Wissinger, B, Hamel, CP, Schorderet, DF, De Baere, E, Sharon, D, Banin, E, Jacobson, SG, Bonneau, D, Zanlonghi, X, Le Meur, G, Casteels, I, Koenekoop, R, Long, VW, Meire, F, Prescott, K, De Ravel, T, Simmons, I, Nguyen, H, Dollfus, H, Poch, O, Léveillard, T, Nguyen-Ba-Charvet, K, Sahel, JA, Bhattacharya, SS & Zeitz, C 2012, 'Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))', American Journal of Human Genetics, vol. 91, no. 1, pp. 209. https://doi.org/10.1016/j.ajhg.2012.06.001

Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330)). / Audo, Isabelle; Bujakowska, Kinga; Orhan, Elise et al.
In: American Journal of Human Genetics, Vol. 91, No. 1, 13.07.2012, p. 209.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))

AU - Audo, Isabelle

AU - Bujakowska, Kinga

AU - Orhan, Elise

AU - Poloschek, Charlotte M.

AU - Defoort-Dhellemmes, Sabine

AU - Drumare, Isabelle

AU - Kohl, Susanne

AU - Luu, Tien D.

AU - Lecompte, Odile

AU - Zrenner, Eberhart

AU - Lancelot, Marie Elise

AU - Antonio, Aline

AU - Germain, Aurore

AU - Michiels, Christelle

AU - Audier, Claire

AU - Letexier, Mélanie

AU - Saraiva, Jean Paul

AU - Leroy, Bart P.

AU - Munier, Francis L.

AU - Mohand-Saïd, Saddek

AU - Lorenz, Birgit

AU - Friedburg, Christoph

AU - Preising, Markus

AU - Kellner, Ulrich

AU - Renner, Agnes B.

AU - Moskova-Doumanova, Veselina

AU - Berger, Wolfgang

AU - Wissinger, Bernd

AU - Hamel, Christian P.

AU - Schorderet, Daniel F.

AU - De Baere, Elfride

AU - Sharon, Dror

AU - Banin, Eyal

AU - Jacobson, Samuel G.

AU - Bonneau, Dominique

AU - Zanlonghi, Xavier

AU - Le Meur, Guylene

AU - Casteels, Ingele

AU - Koenekoop, Robert

AU - Long, Vernon W.

AU - Meire, Francoise

AU - Prescott, Katrina

AU - De Ravel, Thomy

AU - Simmons, Ian

AU - Nguyen, Hoan

AU - Dollfus, Hélène

AU - Poch, Olivier

AU - Léveillard, Thierry

AU - Nguyen-Ba-Charvet, Kim

AU - Sahel, José Alain

AU - Bhattacharya, Shomi S.

AU - Zeitz, Christina

PY - 2012/7/13

Y1 - 2012/7/13

UR - https://www.scopus.com/pages/publications/84863968689

U2 - 10.1016/j.ajhg.2012.06.001

DO - 10.1016/j.ajhg.2012.06.001

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.comment???

AN - SCOPUS:84863968689

SN - 0002-9297

VL - 91

SP - 209

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 1

ER -

Audo I, Bujakowska K, Orhan E, Poloschek CM, Defoort-Dhellemmes S, Drumare I et al. Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330)). American Journal of Human Genetics. 2012 Jul 13;91(1):209. doi: 10.1016/j.ajhg.2012.06.001

Erratum: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (American Journal of Human Genetics (2012) 90 (321-330))

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