Molecular diagnosis of Wilson disease

Molecular Genetics and Metabolism

Volumn 72, Issue 3, 2001, Pages 223-230

  Butler, Patrice ^a   McIntyre, Neil ^a   Mistry, Pramod K ^a  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

ATP7B; Diagnosis; Genotype; Heterozygote; Mutation; Phenotype; Wilson

Indexed keywords

PENICILLAMINE;

ADULT; ALLELE; ARTICLE; CHILD; CLINICAL ARTICLE; DIAGNOSTIC TEST; DNA DETERMINATION; ETHNOLOGY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HETEROZYGOSITY; HUMAN; MALE; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; SINGLE STRAND CONFORMATION POLYMORPHISM; WILSON DISEASE;

EID: 0035716450     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1006/mgme.2000.3143     Document Type: Article

References (28)

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