Severe classical congenital muscular dystrophy and merosin expression-Reference-Cited by-同舟云学术

Severe classical congenital muscular dystrophy and merosin expression

Published:2008-04-23 Issue:3 Volume:54 Page:193-198
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Vajsar Jiri,Chitayat David,Becker Laurence E.,Ho Michael,Ben-Zeev Bruria,Jay Venita

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb04283.x/fullpdf

Reference29 articles.

1. Congenital muscular dystrophy: a clinicopathologic report of 24 cases;McMenamin;J Peds,1982

2. Congenital muscular dystrophy with merosin deficiency;Tome;CR Acad Sci Paris,1994

3. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle;Philpot;Neuromusc Disord,1995

4. Pa-vanello RC. Passos-Bueno MR, Zatz M, Deficiency of merosin (Laminin M or α2) in congenital muscular dystrophy associated with cerebral white matter alterations;Vainzof;Neu-ropediatrics,1995

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1. Merosin-deficient congenital muscular dystrophy in Korea;Brain and Development;2009-05

2. Walker-Warburg syndrome;Orphanet Journal of Rare Diseases;2006-08-03

3. Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagents;Clinical Biochemistry;2003-07

4. Congenital Muscular Dystrophy in Israeli Families;Journal of Child Neurology;2002-05

5. Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome;Pediatric Neurology;2000-02