The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor

EMBO Journal

Volumn 15, Issue 12, 1996, Pages 2914-2923

  Yahraus, Tami ^a   Braverman, Nancy ^a   Dodt, Gabriele ^a   Kalish, Jennifer E ^a   Morrell, James C ^a   Moser, Hugo W ^a   Valle, David ^a   Gould, Stephen J ^a  

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

Author keywords

AAA protein; Expressed sequence tag; Protein import; Zellweger syndrome

Indexed keywords

ADENOSINE TRIPHOSPHATASE; CELL ENZYME; CELL RECEPTOR; CYTOPLASM PROTEIN;

ARTICLE; BIOGENESIS; CONTROLLED STUDY; DISORDERS OF PEROXISOMAL FUNCTIONS; ENDOMYCETALES; FIBROBLAST; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; PEROXISOME; PEROXISOME BIOGENESIS DISORDER; PRIORITY JOURNAL; PROTEIN TRANSPORT; RECESSIVE INHERITANCE;

EID: 0029888487     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.1460-2075.1996.tb00654.x     Document Type: Article

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