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. 2017 Mar 10;26(2):466. doi: 10.1093/hmg/ddw424

Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2

Stylianos Michalakis 1, Lior Shaltiel 1, Vithiyanjali Sothilingam 2, Susanne Koch 1, Verena Schludi 1, Stefanie Krause 1, Christina Zeitz 3,4,5, Isabelle Audo 3,4,5,6,7, Marie-Elise Lancelot 3,4,5, Christian Hamel 8, Isabelle Meunier 8, Markus N Preising 9, Christoph Friedburg 9, Birgit Lorenz 9, Nawal Zabouri 10, Silke Haverkamp 10, Marina Garcia Garrido 2, Naoyuki Tanimoto 2, Mathias W Seeliger 2, Martin Biel 1, Christian A Wahl-Schott 1,*
PMCID: PMC7190878  PMID: 28365780

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).


Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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