The pathological spectrum associated with mutations in the skeletal muscle ryanodine receptor (RYR1) gene

被引：0
|
作者：
Sewry, C. [1 ]
Jungbluth, H. [1 ]
Feng, L. [1 ]
Muntoni, F. [1 ]
机构：
[1] St Thomas Hosp, Dept Paediat Neurol, Evelina Childrens Hosp, London, England
来源：
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY | 2011年 / 37卷
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R74 [神经病学与精神病学];
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页码：30 / 30
页数：1
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