Investigation of mitochondrial function in hereditary spastic paraparesis

NeuroReport

Volumn 14, Issue 3, 2003, Pages 485-488

  McDermott, C J ^a   Taylor, R W ^b   Hayes, C ^b   Johnson, M ^b   Bushby, K M D ^b   Turnbull, D M ^b   Shaw, P J ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

Hereditary spastic paraparesis; Mitochondria; Spastin

Indexed keywords

SPASTIN;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HISTOCHEMISTRY; HUMAN; MITOCHONDRIAL RESPIRATION; MITOCHONDRION; MUSCLE TISSUE; PARAPLEGIN GENE; PATHOGENESIS; PRIORITY JOURNAL; SPECTROPHOTOMETRY;

EID: 0344837697     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001756-200303030-00038     Document Type: Article

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