G.P.1.03 King-Denborough syndrome associated with mutations in the skeletal muscle ryanodine receptor ( RYR1 ) gene

G.P.1.03 King-Denborough syndrome associated with mutations in the skeletal muscle ryanodine receptor ( RYR1 ) gene

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Bibliographic Details
Published in:Neuromuscular disorders : NMD Vol. 19; no. 8; pp. 556 - 557
Main Authors: Dowling, J, Lillis, S, Amburgey, K, Leber, S, Zhou, H, Al-Sarraj, S, Wraige, E, Abbs, S, Sewry, C, 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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Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0960-8966
1873-2364
DOI:10.1016/j.nmd.2009.06.045