Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders

Nature Genetics

Volumn 15, Issue 4, 1997, Pages 385-388

  Chang, Chia Che ^a   Lee, Wen Hui ^a   Moser, Hugo ^a   Valle, David ^a   Gould, Stephen J ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PEROXISOME PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; CAENORHABDITIS ELEGANS; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DATA BASE; DISORDERS OF PEROXISOMAL FUNCTIONS; DNA SEQUENCE; GENE ISOLATION; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SACCHAROMYCES CEREVISIAE; SKIN FIBROBLAST;

AMINO ACID SEQUENCE; BASE SEQUENCE; CELL MEMBRANE; CELLS, CULTURED; CLONING, MOLECULAR; DNA, COMPLEMENTARY; FIBROBLASTS; FRAMESHIFT MUTATION; GENE EXPRESSION; HUMANS; MEMBRANE PROTEINS; MICROBODIES; MOLECULAR SEQUENCE DATA; PEROXISOMAL DISORDERS; SEQUENCE HOMOLOGY, AMINO ACID;

CAENORHABDITIS ELEGANS; SACCHAROMYCES CEREVISIAE;

EID: 0030951104     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0497-385     Document Type: Article

References (19)

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