Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

American Journal of Human Genetics

Volumn 70, Issue 5, 2002, Pages 1328-1332

  Hansen, Jens Jacob ^a   Dürr, Alexandra ^a   Cournu Rebeix, Isabelle ^a   Georgopoulos, Costa ^a   Ang, Debbie ^a   Nielsen, Marit Nyholm ^a   Davoine, Claire Sophie ^a   Brice, Alexis ^a   Fontaine, Bertrand ^a   Gregersen, Niels ^a   Bross, Peter ^a  

^a AARHUS UNIVERSITY HOSPITAL   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONIN; GENE PRODUCT; HEAT SHOCK PROTEIN 60; PROTEIN SPG13; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2Q; CHROMOSOME MAP; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; ESCHERICHIA COLI; FRANCE; GENE DELETION; GENE MUTATION; HEREDITY; HUMAN; HUMAN TISSUE; MITOCHONDRION; PRIORITY JOURNAL; SPASTIC PARAPLEGIA;

ESCHERICHIA COLI;

EID: 0036241765     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/339935     Document Type: Article

References (13)

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12. 7chaperonin complex
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