Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 15, 1998, Pages 8630-8635

  Geisbrecht, Brian V ^a   Collins, Cynthia S ^a   Reuber, Bernadette E ^a   Gould, Stephen J ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE;

ADRENOLEUKODYSTROPHY; BIOGENESIS; CONFERENCE PAPER; GENE MUTATION; GENE OVEREXPRESSION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; MISSENSE MUTATION; PEROXISOME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; REFSUM DISEASE; ZELLWEGER SYNDROME;

EID: 0032555273     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.15.8630     Document Type: Article

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