Inherited disorders of sarcomeric proteins

被引：18

作者：

Laing, NG ^{[1
]}

机构：

[1] Univ Western Australia, Queen Elizabeth II Med Ctr, Ctr Neuromuscular & Neurol Disorders, Austraslian Neuromuscular Res Inst, Nedlands, WA 6009, Australia

来源：

CURRENT OPINION IN NEUROLOGY | 1999年 / 12卷 / 05期

关键词：

D O I：

10.1097/00019052-199910000-00004

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The most important advances in sarcomeric protein diseases continue to be the identification of mutated genes responsible for human diseases. These have recently included those that encode skeletal muscle alpha-actin in autosomal dominant and autosomal recessive nemaline myopathy, nebulin and slow alpha-tropomyosin in autosomal recessive nemaline myopathy, and desmin and alpha B-crystallin in desminopathies. Curr Opin Neurol 12:513-518 (C) 1999 Lippincott Williams & Wilkins.

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页码：513 / 518

页数：6

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