Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry-Reference-Cited by-同舟云学术

Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry

Published:1996-11 Issue:11 Volume:155 Page:968-976
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Herrmann R.,Straub V.,Meyer K.,Kahn T.,Wagner M.,Voit T.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF02282889.pdf

Reference31 articles.

1. Arahata K, Hayashi YK, Koga R et al. (1993) Laminin in animal models for muscular dystrophy: defect of laminin M in skeletal and cardiac muscles and peripheral nerve of the homozygous dystrophic dy/dy mice. Proc Jpn Acad 69:259–264

2. Brown JC, Timpl R (1994) The laminins. Matrix Biol 14: 275–281

3. Campbell KP, Ervasti JM (1993) A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol 122:809–823

4. Dubowitz V (1994) Workshop report on 22nd ENMC sponsored meeting on congential muscular dystrophy held in Baarn, The Netherlands, May 14–16 1993. Neuromusc Disord 4: 75–81

5. Ehrig K, Leivo I, Agraves WS, Ruoslahti E, Engvall E (1990) Merosin, a tissue-specific basement membrane protein, is a laminin-like protein. Proc Natl Acad Sci USA 87: 3264–3268

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