Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles

Annals of Neurology

Volumn 44, Issue 2, 1998, Pages 242-248

  Darin, N ^a   Kyllerman, M ^a   Wahlstrom J ^a   Martinsson, T ^a   Oldfors, A ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; DISEASE CLASSIFICATION; HUMAN; HUMAN TISSUE; JOINT CONTRACTURE; MUSCLE ATROPHY; MUSCLE WEAKNESS; MYOPATHY; OPHTHALMOPLEGIA; PRIORITY JOURNAL;

ADULT; BIOPSY; CHILD; CHROMOSOME MAPPING; CONTRACTURE; ELECTROMYOGRAPHY; FEMALE; GENES, DOMINANT; HUMANS; LINKAGE (GENETICS); MALE; MICROFILAMENTS; MICROSCOPY, ELECTRON; MIDDLE AGED; MITOCHONDRIA; MUSCLE WEAKNESS; MUSCLE, SKELETAL; MYOSITIS, INCLUSION BODY; OPHTHALMOPLEGIA; PEDIGREE; SWEDEN;

EID: 0031830345     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410440215     Document Type: Article

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