Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541

Stylianos Michalakis; Lior Shaltiel; Vithiyanjali Sothilingam; Susanne Koch; Verena Schludi; Stefanie Krause; Christina Zeitz; Isabelle Audo; Marie Elise Lancelot; Christian Hamel; Isabelle Meunier; Markus N. Preising; Christoph Friedburg; Birgit Lorenz; Nawal Zabouri; Silke Haverkamp; Marina Garcia Garrido; Naoyuki Tanimoto; Mathias W. Seeliger; Martin Biel; Christian A. Wahl-Schott

doi:10.1093/hmg/ddw424

Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541

Stylianos Michalakis
, Lior Shaltiel
, Vithiyanjali Sothilingam
, Susanne Koch
, Verena Schludi
, Stefanie Krause
, Christina Zeitz
, Isabelle Audo
, Marie Elise Lancelot
, Christian Hamel
, Isabelle Meunier
, Markus N. Preising
, Christoph Friedburg
, Birgit Lorenz
, Nawal Zabouri
, Silke Haverkamp
, Marina Garcia Garrido
, Naoyuki Tanimoto
, Mathias W. Seeliger
, Martin Biel

Christian A. Wahl-Schott^*

^*Corresponding author for this work

Research output: Contribution to journal › Comment/debate

2 Scopus citations

Abstract

Human Molecular Genetics 2014 23:6; pp. 1538-1550; doi:10.1093/hmg/ddt541 The author would like to apologise for an omission in his funding statement, where SFB 870 was not mentioned. The correct funding statement is the following. This has also been corrected online. This work was supported by the Deutsche Forschungsgemeinschaft (DFG) (WA2597/2-11 and SFB 870); Foundation Voir et Entendre (C.Z.), Prix Dalloz for 'la recherche en ophtalmologie' (C.Z.), Ville de Paris and Region Ile de France, LABEX LIFESENSES (reference ANR-10-LABX-65) supported by French state funds managed by the ANR within the Investissements d'Avenir programme (ANR-11-IDEX-0004-0).

Original language	English
Pages (from-to)	466
Number of pages	1
Journal	Human Molecular Genetics
Volume	26
Issue number	2
DOIs	https://doi.org/10.1093/hmg/ddw424
State	Published - 15 Jan 2017
Externally published	Yes

Bibliographical note

Publisher Copyright:
© The Author 2016. Published by Oxford University Press. All rights reserved.

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10.1093/hmg/ddw424

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Michalakis, S., Shaltiel, L., Sothilingam, V., Koch, S., Schludi, V., Krause, S., Zeitz, C., Audo, I., Lancelot, M. E., Hamel, C., Meunier, I., Preising, M. N., Friedburg, C., Lorenz, B., Zabouri, N., Haverkamp, S., Garrido, M. G., Tanimoto, N., Seeliger, M. W., ... Wahl-Schott, C. A. (2017). Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541. Human Molecular Genetics, 26(2), 466. https://doi.org/10.1093/hmg/ddw424

@article{a1167ccab28c4a0cb0575bca832f261e,

title = "Corrigendum to {"}Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2{"} [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541",

abstract = "Human Molecular Genetics 2014 23:6; pp. 1538-1550; doi:10.1093/hmg/ddt541 The author would like to apologise for an omission in his funding statement, where SFB 870 was not mentioned. The correct funding statement is the following. This has also been corrected online. This work was supported by the Deutsche Forschungsgemeinschaft (DFG) (WA2597/2-11 and SFB 870); Foundation Voir et Entendre (C.Z.), Prix Dalloz for 'la recherche en ophtalmologie' (C.Z.), Ville de Paris and Region Ile de France, LABEX LIFESENSES (reference ANR-10-LABX-65) supported by French state funds managed by the ANR within the Investissements d'Avenir programme (ANR-11-IDEX-0004-0).",

author = "Stylianos Michalakis and Lior Shaltiel and Vithiyanjali Sothilingam and Susanne Koch and Verena Schludi and Stefanie Krause and Christina Zeitz and Isabelle Audo and Lancelot, \{Marie Elise\} and Christian Hamel and Isabelle Meunier and Preising, \{Markus N.\} and Christoph Friedburg and Birgit Lorenz and Nawal Zabouri and Silke Haverkamp and Garrido, \{Marina Garcia\} and Naoyuki Tanimoto and Seeliger, \{Mathias W.\} and Martin Biel and Wahl-Schott, \{Christian A.\}",

year = "2017",

month = jan,

day = "15",

doi = "10.1093/hmg/ddw424",

language = "אנגלית",

volume = "26",

pages = "466",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "2",

}

Michalakis, S, Shaltiel, L, Sothilingam, V, Koch, S, Schludi, V, Krause, S, Zeitz, C, Audo, I, Lancelot, ME, Hamel, C, Meunier, I, Preising, MN, Friedburg, C, Lorenz, B, Zabouri, N, Haverkamp, S, Garrido, MG, Tanimoto, N, Seeliger, MW, Biel, M & Wahl-Schott, CA 2017, 'Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541', Human Molecular Genetics, vol. 26, no. 2, pp. 466. https://doi.org/10.1093/hmg/ddw424

Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541. / Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali et al.
In: Human Molecular Genetics, Vol. 26, No. 2, 15.01.2017, p. 466.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi

T2 - 10.1093/hmg/ddt541

AU - Michalakis, Stylianos

AU - Shaltiel, Lior

AU - Sothilingam, Vithiyanjali

AU - Koch, Susanne

AU - Schludi, Verena

AU - Krause, Stefanie

AU - Zeitz, Christina

AU - Audo, Isabelle

AU - Lancelot, Marie Elise

AU - Hamel, Christian

AU - Meunier, Isabelle

AU - Preising, Markus N.

AU - Friedburg, Christoph

AU - Lorenz, Birgit

AU - Zabouri, Nawal

AU - Haverkamp, Silke

AU - Garrido, Marina Garcia

AU - Tanimoto, Naoyuki

AU - Seeliger, Mathias W.

AU - Biel, Martin

AU - Wahl-Schott, Christian A.

PY - 2017/1/15

Y1 - 2017/1/15

N2 - Human Molecular Genetics 2014 23:6; pp. 1538-1550; doi:10.1093/hmg/ddt541 The author would like to apologise for an omission in his funding statement, where SFB 870 was not mentioned. The correct funding statement is the following. This has also been corrected online. This work was supported by the Deutsche Forschungsgemeinschaft (DFG) (WA2597/2-11 and SFB 870); Foundation Voir et Entendre (C.Z.), Prix Dalloz for 'la recherche en ophtalmologie' (C.Z.), Ville de Paris and Region Ile de France, LABEX LIFESENSES (reference ANR-10-LABX-65) supported by French state funds managed by the ANR within the Investissements d'Avenir programme (ANR-11-IDEX-0004-0).

AB - Human Molecular Genetics 2014 23:6; pp. 1538-1550; doi:10.1093/hmg/ddt541 The author would like to apologise for an omission in his funding statement, where SFB 870 was not mentioned. The correct funding statement is the following. This has also been corrected online. This work was supported by the Deutsche Forschungsgemeinschaft (DFG) (WA2597/2-11 and SFB 870); Foundation Voir et Entendre (C.Z.), Prix Dalloz for 'la recherche en ophtalmologie' (C.Z.), Ville de Paris and Region Ile de France, LABEX LIFESENSES (reference ANR-10-LABX-65) supported by French state funds managed by the ANR within the Investissements d'Avenir programme (ANR-11-IDEX-0004-0).

UR - https://www.scopus.com/pages/publications/85018247707

U2 - 10.1093/hmg/ddw424

DO - 10.1093/hmg/ddw424

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

C2 - 28365780

AN - SCOPUS:85018247707

SN - 0964-6906

VL - 26

SP - 466

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 2

ER -

Corrigendum to "Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2" [Human Molecular Genetics 2014, 23:6:1538-1550]; doi: 10.1093/hmg/ddt541

Abstract

Bibliographical note

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