SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

Nature Genetics

Volumn 20, Issue 4, 1998, Pages 337-343

  Zhu, Zhiqing ^a   Yao, Jianbo ^a   Johns, Timothy ^a   Fu, Katherine ^a   De Bie, Isabelle ^a   Macmillan, Carol ^a   Cuthbert, Andrew P ^c   Newbold, Robert F ^c   Wang, Jia Chi ^d   Chevrette, Mario ^d   Brown, Garry K ^e   Brown, Ruth M ^e   Shoubridge, Eric A ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c BRUNEL UNIVERSITY   (United Kingdom)

^d MONTREAL GENERAL HOSPITAL   (Canada)

^e UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE;

ARTICLE; BIOGENESIS; BRAIN CORTEX; CHROMOSOME 9Q; CHROMOSOME TRANSLOCATION; DNA SEQUENCE; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; LEIGH DISEASE; NERVE DEGENERATION; NEUROLOGIC DISEASE; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; DNA, COMPLEMENTARY; ELECTRON TRANSPORT COMPLEX IV; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEIGH DISEASE; MEMBRANE PROTEINS; MITOCHONDRIAL PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 17344362021     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/3804     Document Type: Article

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