Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders

American Journal of Human Genetics

Volumn 63, Issue 2, 1998, Pages 347-359

  Warren, Daniel S ^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

[No Author keywords available]

Indexed keywords

MATRIX PROTEIN;

ADRENOLEUKODYSTROPHY; ARTICLE; GENE ACTIVITY; GENE MUTATION; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; NUCLEOTIDE SEQUENCE; PEROXISOME; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN TRANSPORT; YEAST; ZELLWEGER SYNDROME;

EID: 0032231872     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301963     Document Type: Article

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