Loss-of-function mutations inSCN4Acause severe foetal hypokinesia or ‘classical’ congenital myopathy-Reference-Cited by-同舟云学术

Loss-of-function mutations inSCN4Acause severe foetal hypokinesia or ‘classical’ congenital myopathy

Published:2015-12-22 Issue:3 Volume:139 Page:674-691
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Zaharieva Irina T.,Thor Michael G.,Oates Emily C.,van Karnebeek Clara,Hendson Glenda,Blom Eveline,Witting Nanna,Rasmussen Magnhild,Gabbett Michael T.,Ravenscroft Gianina,Sframeli Maria,Suetterlin Karen,Sarkozy Anna,D’Argenzio Luigi,Hartley Louise,Matthews Emma,Pitt Matthew,Vissing John,Ballegaard Martin,Krarup Christian,Slørdahl Andreas,Halvorsen Hanne,Ye Xin Cynthia,Zhang Lin-Hua,Løkken Nicoline,Werlauff Ulla,Abdelsayed Mena,Davis Mark R.,Feng Lucy,Phadke Rahul,Sewry Caroline A.,Morgan Jennifer E.,Laing Nigel G.,Vallance Hilary,Ruben Peter,Hanna Michael G.,Lewis Suzanne,Kamsteeg Erik-Jan,Männikkö Roope,Muntoni Francesco

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/139/3/674/17348220/awv352.pdf

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