A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies-Reference-Cited by-同舟云学术

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A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies

Published:1999-12-01 Issue:8 Volume:9 Page:555-563
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:
Short-container-title:

Author:

Richard I

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Calpain-3 mutations in Turkey;European Journal of Pediatrics;2006-01-13

2. Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis;Neuromuscular Disorders;2006-01

3. Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes;Journal of Medical Genetics;2005-09-01

4. A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F;Neuromuscular Disorders;2000-06

5. Calpainopathy—A Survey of Mutations and Polymorphisms;The American Journal of Human Genetics;1999-06

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