Laminin-α2 (merosin), β-dystroglycan, α-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: An immunohistochemical study-Reference-Cited by-同舟云学术

Laminin-α2 (merosin), β-dystroglycan, α-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: An immunohistochemical study

Published:1998-03 Issue:1 Volume:100 Page:5-10
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

ter Laak H.J,Leyten Q.H,Gabreëls F.J.M,Kuppen H,Renier W.O,Sengers R.C.A

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Surgery

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5. Abnormal localization of laminin subunits in muscular dystrophies;Hayashi;J Neurol Sci,1993

Cited by 4 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. Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases;Arquivos de Neuro-Psiquiatria;2005-09

2. The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review;Journal of Medical Genetics;2001-10-01

3. Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy;Brain and Development;2001-03

4. Inherited disorders of the extracellular matrix;Current Opinion in Neurology;1999-10