Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))

Prasanthi Namburi; Rinki Ratnapriya; Samer Khateb; Csilla H. Lazar; Yael Kinarty; Alexey Obolensky; Inbar Erdinest; Devorah Marks-Ohana; Eran Pras; Tamar Ben-Yosef; Hadas Newman; Menachem Gross; Anand Swaroop; Eyal Banin; Dror Sharon

doi:10.1016/j.ajhg.2016.09.012

Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))

Prasanthi Namburi
, Rinki Ratnapriya
, Samer Khateb
, Csilla H. Lazar
, Yael Kinarty
, Alexey Obolensky
, Inbar Erdinest
, Devorah Marks-Ohana
, Eran Pras
, Tamar Ben-Yosef
, Hadas Newman
, Menachem Gross
, Anand Swaroop
, Eyal Banin^*
, Dror Sharon

^*Corresponding author for this work

Institute for Medical Research Israel-Canada (IMRIC)

Research output: Contribution to journal › Comment/debate

14 Scopus citations

Abstract

In the original article, Table 1 included multiple editing errors. The corrected table has been included here and online. The authors regret the error.

Original language	English
Pages (from-to)	1222-1223
Number of pages	2
Journal	American Journal of Human Genetics
Volume	99
Issue number	5
DOIs	https://doi.org/10.1016/j.ajhg.2016.09.012
State	Published - 3 Nov 2016

Bibliographical note

Publisher Copyright:
© 2016 American Society of Human Genetics

Access to Document

10.1016/j.ajhg.2016.09.012

Fingerprint

Dive into the research topics of 'Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))'. Together they form a unique fingerprint.

Cite this

Namburi, P., Ratnapriya, R., Khateb, S., Lazar, C. H., Kinarty, Y., Obolensky, A., Erdinest, I., Marks-Ohana, D., Pras, E., Ben-Yosef, T., Newman, H., Gross, M., Swaroop, A., Banin, E., & Sharon, D. (2016). Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010)). American Journal of Human Genetics, 99(5), 1222-1223. https://doi.org/10.1016/j.ajhg.2016.09.012

Namburi, Prasanthi ; Ratnapriya, Rinki ; Khateb, Samer et al. / Correction : Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010)). In: American Journal of Human Genetics. 2016 ; Vol. 99, No. 5. pp. 1222-1223.

@article{f8de96a19674486cb95f4c709fa2b4f0,

title = "Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))",

abstract = "In the original article, Table 1 included multiple editing errors. The corrected table has been included here and online. The authors regret the error.",

author = "Prasanthi Namburi and Rinki Ratnapriya and Samer Khateb and Lazar, \{Csilla H.\} and Yael Kinarty and Alexey Obolensky and Inbar Erdinest and Devorah Marks-Ohana and Eran Pras and Tamar Ben-Yosef and Hadas Newman and Menachem Gross and Anand Swaroop and Eyal Banin and Dror Sharon",

note = "Publisher Copyright: {\textcopyright} 2016 American Society of Human Genetics",

year = "2016",

month = nov,

day = "3",

doi = "10.1016/j.ajhg.2016.09.012",

language = "אנגלית",

volume = "99",

pages = "1222--1223",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "5",

}

Namburi, P, Ratnapriya, R, Khateb, S, Lazar, CH, Kinarty, Y, Obolensky, A, Erdinest, I, Marks-Ohana, D, Pras, E, Ben-Yosef, T, Newman, H, Gross, M, Swaroop, A, Banin, E & Sharon, D 2016, 'Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))', American Journal of Human Genetics, vol. 99, no. 5, pp. 1222-1223. https://doi.org/10.1016/j.ajhg.2016.09.012

Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010)). / Namburi, Prasanthi; Ratnapriya, Rinki; Khateb, Samer et al.
In: American Journal of Human Genetics, Vol. 99, No. 5, 03.11.2016, p. 1222-1223.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Correction

T2 - Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))

AU - Namburi, Prasanthi

AU - Ratnapriya, Rinki

AU - Khateb, Samer

AU - Lazar, Csilla H.

AU - Kinarty, Yael

AU - Obolensky, Alexey

AU - Erdinest, Inbar

AU - Marks-Ohana, Devorah

AU - Pras, Eran

AU - Ben-Yosef, Tamar

AU - Newman, Hadas

AU - Gross, Menachem

AU - Swaroop, Anand

AU - Banin, Eyal

AU - Sharon, Dror

PY - 2016/11/3

Y1 - 2016/11/3

N2 - In the original article, Table 1 included multiple editing errors. The corrected table has been included here and online. The authors regret the error.

AB - In the original article, Table 1 included multiple editing errors. The corrected table has been included here and online. The authors regret the error.

UR - https://www.scopus.com/pages/publications/84997327963

U2 - 10.1016/j.ajhg.2016.09.012

DO - 10.1016/j.ajhg.2016.09.012

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

AN - SCOPUS:84997327963

SN - 0002-9297

VL - 99

SP - 1222

EP - 1223

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 5

ER -

Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A et al. Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010)). American Journal of Human Genetics. 2016 Nov 3;99(5):1222-1223. doi: 10.1016/j.ajhg.2016.09.012

Correction: Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss (The American Journal of Human Genetics (2016) 99(5) (1222–1223) (S0002929716302841) (10.1016/j.ajhg.2016.07.010))

Abstract

Bibliographical note

Access to Document

Other files and links

Fingerprint

Cite this