A patient with mitochondrial myopathy associated with isolated succinate dehydrogenase deficiency

Brain and Development

Volumn 22, Issue 3, 2000, Pages 158-162

  Sugimoto, Junko ^a   Shimohira, Masayuki ^a   Osawa, Yukiko ^a   Matsubara, Masaaki ^a   Yamamoto, Haruyasu ^a   Goto, Yu ichi ^b   Nonaka, Ikuya ^b  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

Congenital dislocation of joints; Hypotonia; Succinate dehydrogenase deficiency

Indexed keywords

CYTOCHROME C OXIDASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; SUCCINATE DEHYDROGENASE;

ARTICLE; CASE REPORT; DISEASE ASSOCIATION; ENZYME DEFICIENCY; HUMAN; HUMAN TISSUE; JOINT DISLOCATION; MALE; MITOCHONDRIAL MYOPATHY; MUSCLE BIOPSY; MUSCLE HYPOTONIA; PRESCHOOL CHILD;

BIOPSY; BRAIN; HUMANS; INFANT; INTELLIGENCE TESTS; JOINT INSTABILITY; MAGNETIC RESONANCE IMAGING; MALE; MITOCHONDRIAL MYOPATHIES; MUSCLE HYPOTONIA; MUSCLE, SKELETAL; SUCCINATE DEHYDROGENASE;

EID: 0034709403     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(00)00097-8     Document Type: Article

References (11)

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