X-linked adrenoleukodystrophy: Genes, mutations, and phenotypes

Neurochemical Research

Volumn 24, Issue 4, 1999, Pages 521-535

  Smith, Kirby D ^a,b   Kemp, Stephan ^a   Braiterman, Lelita T ^a   Lu, Jyh Feng ^a   Wei, He Ming ^a   Geraghty, Michael ^a   Stetten, Gail ^a   Bergin, James S ^a   Pevsner, Jonathan ^a   Watkins, Paul A ^a  

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

^b KENNEDY KRIEGER INSTITUTE   (United States)

Author keywords

ABC transporters; Adrenoleukodystrophy; Genotype phenotype; Mutations; Peroxisomes; VLCS

Indexed keywords

ABC TRANSPORTER;

ADRENOLEUKODYSTROPHY; ARTICLE; CLINICAL FEATURE; GENE MUTATION; GENOTYPE; HUMAN; MISSENSE MUTATION; MOLECULAR EVOLUTION; PHENOTYPE; PHYLOGENY; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

EID: 0032893407     PISSN: 03643190     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1022535930009     Document Type: Article

References (76)

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