TPM3 MUTATION IN ONE OF THE ORIGINAL CASES OF CAP DISEASE

被引：32

作者：

Ohlsson, Monica

Fidzianska, Anna

Tajsharghi, Homa

Oldfors, Anders

机构：

[1] Department of Pathology, Sahlgrenska University Hospital, Goteborg

[2] Neuromuscular Unit, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw

[3] Department of Pathology, Sahlgrenska University Hospital

来源：

NEUROLOGY | 2009年 / 72卷 / 22期

关键词：

TROPOMYOSIN GENE TPM2; CONGENITAL MYOPATHY;

D O I：

10.1212/WNL.0b013e3181a82659

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

100204 [神经病学];

摘要：

[No abstract available]

引用

页码：1961 / 1963

页数：7

共 7 条

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New morphologic and genetic findings in cap disease associated with β-tropomyosin (TPM2) mutations [J].

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[6]

A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation:: A clinical and pathological study [J].

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[7]

Congenital myopathy with nemaline rods and cap structures caused by a mutation in the β-tropomyosin gene (TPM2) [J].

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