Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutant. | Neuromuscul Disord;13(5): 376-87, 2003 Jun. | MEDLINE

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Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutant.

Raymackers, J M; Debaix, H; Colson-Van Schoor, M; De Backer, F; Tajeddine, N; Schwaller, B; Gailly, P; Gillis, J M.

Affiliation

Raymackers JM; Department of Physiology and Pharmacology, Catholic University of Louvain, B-1200 Brussels, Belgium.

Neuromuscul Disord ; 13(5): 376-87, 2003 Jun.

Article in En | MEDLINE | ID: mdl-12798793

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Parvalbumins / Phenotype / Calcium / Dystrophin / Muscle, Skeletal / Mutation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2003 Document type: Article Affiliation country: Bélgica

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Collection: 01-internacional Database: MEDLINE Main subject: Parvalbumins / Phenotype / Calcium / Dystrophin / Muscle, Skeletal / Mutation Type of study: Prognostic_studies Limits: Animals Language: En Journal: Neuromuscul Disord Journal subject: NEUROLOGIA Year: 2003 Document type: Article Affiliation country: Bélgica