X-linked myopathy with excessive autophagy: a new hereditary muscle disease.

Kalimo, H; Savontaus, M L; Lang, H; Paljärvi, L; Sonninen, V; Dean, P B; Katevuo, K; Salminen, A

Kalimo, H; Savontaus, M L; Lang, H; Paljärvi, L; Sonninen, V; Dean, P B; Katevuo, K; Salminen, A.

Affiliation

Kalimo H; Department of Pathology, University of Turku, Finland.

Ann Neurol ; 23(3): 258-65, 1988 Mar.

Article in En | MEDLINE | ID: mdl-2897824

Subject(s)

Autophagy; Genetic Linkage; Muscle Hypotonia/genetics; Muscular Atrophy/genetics; Phagocytosis; Sex Chromosome Aberrations/genetics; X Chromosome; Adult; Biopsy; Genes, Recessive; Humans; Male; Microscopy, Electron; Muscle Hypotonia/pathology; Muscles/pathology; Muscular Atrophy/pathology; Pedigree; Polymorphism, Restriction Fragment Length; Tomography, X-Ray Computed

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Collection: 01-internacional Database: MEDLINE Main subject: Phagocytosis / Sex Chromosome Aberrations / Autophagy / X Chromosome / Muscular Atrophy / Genetic Linkage / Muscle Hypotonia Limits: Adult / Humans / Male Language: En Journal: Ann Neurol Year: 1988 Document type: Article

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