Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia-Reference-Cited by-同舟云学术

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia

Published:2012-09-09 Issue:10 Volume:44 Page:1080-1083
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Zimoń Magdalena,Baets Jonathan,Almeida-Souza Leonardo,De Vriendt Els,Nikodinovic Jelena,Parman Yesim,Battaloǧlu Esra,Matur Zeliha,Guergueltcheva Velina,Tournev Ivailo,Auer-Grumbach Michaela,De Rijk Peter,Petersen Britt-Sabina,Müller Thomas,Fransen Erik,Van Damme Philip,Löscher Wolfgang N,Barišić Nina,Mitrovic Zoran,Previtali Stefano C,Topaloǧlu Haluk,Bernert Günther,Beleza-Meireles Ana,Todorovic Slobodanka,Savic-Pavicevic Dusanka,Ishpekova Boryana,Lechner Silvia,Peeters Kristien,Ooms Tinne,Hahn Angelika F,Züchner Stephan,Timmerman Vincent,Van Dijck Patrick,Rasic Vedrana Milic,Janecke Andreas R,De Jonghe Peter,Jordanova Albena

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2406.pdf

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