RYR1 mutations are a common cause of congenital myopathies with central nuclei-Reference-Cited by-同舟云学术

RYR1 mutations are a common cause of congenital myopathies with central nuclei

Published:2010-09-13 Issue:5 Volume:68 Page:717-726
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Wilmshurst J.M.,Lillis S.,Zhou H.,Pillay K.,Henderson H.,Kress W.,Müller C.R.,Ndondo A.,Cloke V.,Cullup T.,Bertini E.,Boennemann C.,Straub V.,Quinlivan R.,Dowling J.J.,Al- Sarraj S.,Treves S.,Abbs S.,Manzur A.Y.,Sewry C.A.,Muntoni F.,Jungbluth H.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.22119/fullpdf

Reference44 articles.

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4. Mutations in dynamin 2 cause dominant centronuclear myopathy;Bitoun;Nat Genet,2005

5. Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset;Bitoun;Ann Neurol,2007

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