Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G

American Journal of Human Genetics

Volumn 67, Issue 4, 2000, Pages 967-975

  Muntau, Ania C ^a   Mayerhofer, Peter U ^a   Paton, Barbara C ^b   Kammerer, Stefan ^c   Roscher, Adelbert A ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^b WOMEN S AND CHILDREN S HOSPITAL   (Australia)

^c SEQUENOM INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CELL FUSION; GENE MUTATION; HUMAN; HUMAN CELL; MEMBRANE; MEMBRANE STRUCTURE; PEROXISOME; PRIORITY JOURNAL; ZELLWEGER SYNDROME;

EID: 0033794897     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303071     Document Type: Article

References (26)

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