Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

Nature Genetics

Volumn 17, Issue 4, 1997, Pages 449-450

  Portsteffen, Herma ^a   Beyer, Andreas ^a   Becker, Elisabeth ^a   Epplen, Cornelia ^a   Pawlak, André ^b   Kunau, Wolf H ^a   Dodt, Gabriele ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b HENRI MONDOR HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; COMPLEMENTARY DNA;

ADRENOLEUKODYSTROPHY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BIOGENESIS; FIBROBLAST; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; MUTATION; NONHUMAN; PEROXISOME; PRIORITY JOURNAL; REFSUM DISEASE; SACCHAROMYCES CEREVISIAE; ZELLWEGER SYNDROME;

SACCHAROMYCES CEREVISIAE;

EID: 0030720859     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1297-449     Document Type: Article

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