Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

David N Herrmann; Rita Horvath; Janet E Sowden; Michael Gonzalez; Avencia Sanchez-Mejias; Zhuo Guan; Roger G Whittaker; Jorge L Almodovar; Maria Lane; Boglarka Bansagi; Angela Pyle; Veronika Boczonadi; Hanns Lochmüller; Helen Griffin; Patrick F Chinnery; Thomas E Lloyd; J. Troy Littleton; Stephan Zuchner

doi:10.1016/j.ajhg.2014.09.012

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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

David N Herrmann, Rita Horvath, Janet E Sowden, Michael Gonzalez, Avencia Sanchez-Mejias, Zhuo Guan, Roger G Whittaker, Jorge L Almodovar, Maria Lane, Boglarka Bansagi, …

American journal of human genetics, Vol.95(4), pp.472-472

2014-10-02

DOI: https://doi.org/10.1016/j.ajhg.2014.09.012

PMCID: PMC4157148

PMID: 25192047

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Title: Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy
Creators: David N Herrmann
Rita Horvath
Janet E Sowden
Michael Gonzalez
Avencia Sanchez-Mejias
Zhuo Guan
Roger G Whittaker
Jorge L Almodovar
Maria Lane
Boglarka Bansagi
Angela Pyle
Veronika Boczonadi
Hanns Lochmüller
Helen Griffin
Patrick F Chinnery
Thomas E Lloyd
J. Troy Littleton
Stephan Zuchner
Publication Details: American journal of human genetics, Vol.95(4), pp.472-472
Publisher: Elsevier
Academic Unit: Leadership Department; Miller School of Medicine; John P. Hussman Institute for Human Genomics
Language: English
Resource Type: Journal article
PMID: 25192047
PMCID: PMC4157148
Record Identifier: 991031619692402976