Simultaneous detection of C282Y and H63D hemochromatosis mutations by dual-color probes

Molecular Diagnosis

Volumn 5, Issue 2, 2000, Pages 107-116

  Lyon, Elaine ^a  

^a ARUP LABORATORIES   (United States)

Author keywords

Fluorescent hybridization probes; Melting curve analysis; Mutation detection

Indexed keywords

FLUORESCEIN; LYSINE; THREONINE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; BASE MISPAIRING; CONTROLLED STUDY; FLUORESCENCE; GENE MUTATION; GENOTYPE; HEMOCHROMATOSIS; HUMAN; POLYMERASE CHAIN REACTION;

EID: 0033934164     PISSN: 10848592     EISSN: None     Source Type: Journal    
DOI: 10.2165/00066982-200005020-00004     Document Type: Article

References (2)

1. McLaren CE, Gordeuk VR, Looker AC, et al.: Prevalence of heterozygotes for hemochromatosis in the white population of the United States. Blood 1995;86:2021-2027
2. Feder JN, Gnirke A, Thomas W, et al.: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;13: 399-408