Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers-Reference-Cited by-同舟云学术

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Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers

Published:1993-01 Issue:2 Volume:3 Page:135-140
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Vainzof Mariz,Nicholson Louise V.B.,Bulman Dennis E.,Tsanaclis Ana Maria,Passos-Bueno Maria Rita,Pavanello Rita C.M.,Zatz Mayana

Publisher

Elsevier BV

Subject

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

Reference26 articles.

1. Dystrophy: the protein product of the Duchenne muscular dystrophin locus;Hoffman;Cell,1987

2. Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophin;Hoffman;N Engl J Med,1988

3. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle;Zubrzycka-Gaarn;Nature,1988

4. Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophin;Nicholson;J Neurol Sci,1989

5. Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy;Nicholson;Acta Neuropathol,1990

Cited by 3 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. Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene;Neuromuscular Disorders;2001-07

2. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin–glycoprotein complex;European Journal of Human Genetics;1999-03

3. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers;American Journal of Medical Genetics;1998-12-04

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