Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice-Reference-Cited by-同舟云学术

Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice

Published:2001-11 Issue:8 Volume:11 Page:703-712
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Connolly Anne M,Keeling Richard M,Mehta Shobhna,Pestronk Alan,Sanes Joshua R

Publisher

Elsevier BV

Subject

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

Reference70 articles.

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3. The molecular basis of muscular dystrophy in the mdx mouse: a point mutation;Sicinski;Science,1989

4. Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy;Deconinck;Cell,1997

5. Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy;Grady;Cell,1997

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