G.P.1.04 An autosomal-recessive form of centronuclear myopathy is caused by mutations in the skeletal muscle ryanodine receptor ( RYR1 ) gene

G.P.1.04 An autosomal-recessive form of centronuclear myopathy is caused by mutations in the skeletal muscle ryanodine receptor ( RYR1 ) gene

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Bibliographic Details
Published in:Neuromuscular disorders : NMD Vol. 19; no. 8; p. 557
Main Authors: Wilmshurst, J, Lillis, S, Zhou, H, Kress, W, Solomon, R, Ndondo, A, Greenberg, J, Sinclair-Smith, C.C, Bertini, E, Boennemann, C, Straub, V, Quinlivan, R, Sewry, C.A, Wraige, E, Abbs, S, Muntoni, F, Jungbluth, H
Format: Journal Article
Language:English
Published: Elsevier B.V 01-09-2009
Subjects:
Neurology
Online Access:Get full text
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Description
ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2009.06.046