Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1

Journal of the Neurological Sciences

Volumn 144, Issue 1-2, 1996, Pages 91-98

  Forsgren, Lars ^a   Libelius, Rolf ^a   Holmberg, Monica ^a   Döbeln, Ulrika von ^a   Wibom, Rolf ^a   Heijbel, Jan ^a   Sandgren, Ola ^b   Holmgren, Gösta ^a  

^a UMEÅ UNIVERSITY HOSPITAL   (Sweden)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

anticipation; dominant ataxia; infantile form; mitochondrial activity; muscle morphology; olivopontocerebellar atrophy; retinal degeneration

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL DOMINANT DISORDER; BRAIN ATROPHY; CHILD; CHROMOSOME 3P; CLINICAL ARTICLE; DYSARTHRIA; HEREDITARY ATAXIA; HISTOCHEMISTRY; HUMAN; MITOCHONDRIAL RESPIRATION; MUSCLE MITOCHONDRION; PRIORITY JOURNAL; RETINA DEGENERATION;

ADULT; AGED; CEREBELLAR ATAXIA; CHROMOSOMES, HUMAN, PAIR 3; FEMALE; GENES, DOMINANT; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MICROSCOPY, ELECTRON; MIDDLE AGED; MITOCHONDRIA, MUSCLE; MUSCLES; RETINAL DEGENERATION; SWEDEN;

EID: 0030471959     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(96)00187-6     Document Type: Article

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