Autosomal centronuclear myopathy due to mutations in the skeletal muscle ryanodine receptor gene

被引：0

作者：

Jungbluth, H

Zhou, H

Bertini, E

Straub, V

Bushby, K

Robb, S

Treves, S

Sewry, C

Muntoni, F

机构：

[1] Hammersmith Hosp, Dubowitz Neuromuscular Ctr, London, England

[2] Guys Hosp, Dept Paediat Neurol, London SE1 9RT, England

[3] Osped Bambino Gesu, Rome, Italy

[4] Univ Newcastle Upon Tyne, Int Ctr Life, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

[5] Kantonsspital Basel, Dept Anaesthesia & Res, Basel, Switzerland

[6] Robert Jones & Agnes Hunt Orthopaed Hosp, Ctr Inherited Neuromuscular Disorders, Oswestry SY10 7AG, Shrops, England

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D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：30 / 31

页数：2