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.
N1 - Publisher Copyright:
© The Author 2016. Published by Oxford University Press. All rights reserved.
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 - http://www.scopus.com/inward/record.url?scp=85018247707&partnerID=8YFLogxK
U2 - 10.1093/hmg/ddw424
DO - 10.1093/hmg/ddw424
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C2 - 28365780
AN - SCOPUS:85018247707
SN - 0964-6906
VL - 26
SP - 466
JO - Human Molecular Genetics
JF - Human Molecular Genetics
IS - 2
ER -