Loss of dystrophin and β-sarcoglycan significantly exacerbates the phenotype of laminin α2 chain-deficient animals

American Journal of Pathology

Volumn 184, Issue 3, 2014, Pages 740-752

  Gawlik, Kinga I ^a   Holmberg, Johan ^a   Durbeej, Madeleine ^a  

^a LUND UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; LAMININ; LAMININ ALPHA2; SARCOGLYCAN;

ANIMAL; ANIMAL MUSCULAR DYSTROPHY; DEFICIENCY; DISEASE MODEL; FEMALE; GENETICS; KNOCKOUT MOUSE; MALE; METABOLISM; MOUSE; PATHOLOGY; PHENOTYPE; REGENERATION; SKELETAL MUSCLE; SKELETAL MUSCLE CELL; X CHROMOSOME LINKED MUSCULAR DYSTROPHIC MOUSE;

ANIMALS; DISEASE MODELS, ANIMAL; DYSTROPHIN; FEMALE; LAMININ; MALE; MICE; MICE, INBRED MDX; MICE, KNOCKOUT; MUSCLE FIBERS, SKELETAL; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, ANIMAL; PHENOTYPE; REGENERATION; SARCOGLYCANS;

EID: 84894126274     PISSN: 00029440     EISSN: 15252191     Source Type: Journal    
DOI: 10.1016/j.ajpath.2013.11.017     Document Type: Article

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