Haplotype studies in Wilson disease.
In 51 families with Wilson disease, we have studied DNA haplotypes of dinucleotide repeat polymorphisms (CA repeats) in the 13q14.3 region, to examine these markers for association with the Wilson disease gene (WND). In addition to a marker (D13S133) described elsewhere, we have developed three new...
المؤلفون الرئيسيون: | Thomas, G, Bull, P, Roberts, E, Walshe, J, Cox, D |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
1994
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مواد مشابهة
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HAPLOTYPES IN WILSON DISEASE - IMPLICATIONS FOR MUTATIONAL ANALYSIS
حسب: Thomas, G, وآخرون
منشور في: (1993) -
Wilson disease and Menkes disease: new handles on heavy-metal transport.
حسب: Bull, P, وآخرون
منشور في: (1994) -
PHYSICAL MAPPING OF 13Q14.3 FOCUSED ON THE REGION OF THE WILSON DISEASE LOCUS
حسب: Bull, P, وآخرون
منشور في: (1993) -
REGIONAL LOCALIZATION OF CHROMOSOME-13 CLONES AND THEIR APPLICATION TO WILSON DISEASE
حسب: Bull, P, وآخرون
منشور في: (1991) -
Long range restriction mapping of 13q14.3 focused on the Wilson disease region.
حسب: Bull, P, وآخرون
منشور في: (1993)