Friedreich's ataxia protein: Phylogenetic evidence for mitochondrial dysfunction

Trends in Neurosciences

Volumn 19, Issue 11, 1996, Pages 465-468

  Gibson, Toby J ^a   Koonin, Eugene V ^b   Musco, Giovanna ^a   Pastore, Annalisa ^a   Bork, Peer ^a,c  

^a EUROPEAN MOLECULAR BIOLOGY LABORATORY   (Germany)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

^c MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; FRIEDREICH ATAXIA; HUMAN; MITOCHONDRION; NEUROPATHY; NONHUMAN; PRIORITY JOURNAL; VITAMIN DEFICIENCY;

AMINO ACID SEQUENCE; FRIEDREICH ATAXIA; HUMANS; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; PROTEINS;

EID: 0030296878     PISSN: 01662236     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0166-2236(96)20054-2     Document Type: Article

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