[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].

Fardeau, M; Tomé, F M; Helbling-Leclerc, A; Evangelista, T; Ottolini, A; Chevallay, M; Barois, A; Estournet, B; Harpey, J P; Fauré, S; Guicheney, P; Hillaire, D

[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis]. / Dystrophie musculaire congénitale avec déficience en mérosine: analyse clinique, histopathologique, immunocytochimique et génétique.

Fardeau, M; Tomé, F M; Helbling-Leclerc, A; Evangelista, T; Ottolini, A; Chevallay, M; Barois, A; Estournet, B; Harpey, J P; Fauré, S; Guicheney, P; Hillaire, D.

Affiliation

Fardeau M; INSERM Unité 153, Paris.

Rev Neurol (Paris) ; 152(1): 11-9, 1996 Jan.

Article in Fr | MEDLINE | ID: mdl-8729391

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Collection: 01-internacional Database: MEDLINE Main subject: Laminin / Muscles / Muscular Dystrophies Type of study: Observational_studies / Prognostic_studies Limits: Female / Humans / Male / Newborn Language: Fr Journal: Rev Neurol (Paris) Year: 1996 Document type: Article Country of publication:

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