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Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Muchir, A.
  • 期刊名称Human Molecular Genetics
  • 作者Muchir, A.
  • 卷第9卷
  • 期第9期
  • 电子ISSN1460-2083
  • 文件大小485.14KB
  • 发表时间2000-5-22
  • DOI10.1093/hmg/9.9.1453
  • 页码1453-1459
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