Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy-Reference-Cited by-同舟云学术

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Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy

Published:2002-07 Issue:3 Volume:76 Page:217-224
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Pillers De-Ann M,Kempton J.Beth,Duncan Nancy M,Pang Jiaqing,Dwinnell Shannon J,Trune Dennis R

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference41 articles.

1. Facioscapulohumeral dystrophy associated with Coats syndrome;Taylor;Ann. Neurol.,1982

2. Facioscapulohumeral muscular dystrophy and accompanying hearing loss;Meyerson;Arch. Otolaryngol.,1984

3. Hearing loss in facioscapulohumeral dystrophy;Voit;Eur. J. Pediatr.,1986

4. Hearing loss in fascioscapulohumeral muscular dystrophy;Brouwer;Neurology,1991

5. Facioscapulohumeral muscular dystrophy in early childhood;Brouwer;Arch. Neurol.,1994

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