Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

Acta Neuropathologica

Volumn 100, Issue 1, 2000, Pages 23-28

  Jansson, Monica ^a   Darin, Niklas ^a   Kyllerman, Mårten ^a   Martinsson, Tommy ^a   Wahlström, Jan ^a   Oldfors, Anders ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Cytochrome c oxidase; Hereditary inclusion body myopathy; Mitochondria; Mitochondrial DNA deletions

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CELL INCLUSION; CELL VACUOLE; CLINICAL ARTICLE; CLINICAL FEATURE; DETERIORATION; GENE DELETION; HUMAN; HUMAN CELL; HUMAN TISSUE; IN SITU HYBRIDIZATION; INCLUSION BODY MYOSITIS; JOINT CONTRACTURE; MUSCLE BIOPSY; MUSCLE CELL; MUSCLE FUNCTION; MUSCLE WEAKNESS; MYOPATHY; NUCLEOTIDE REPEAT; OPHTHALMOPLEGIA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; CHILD; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; FEMALE; GENE DELETION; HUMANS; MALE; MIDDLE AGED; MUSCLE FIBERS; MUSCLE, SKELETAL; MYOSITIS, INCLUSION BODY; PEDIGREE;

EID: 0034083020     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010051188     Document Type: Article

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