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Heterogeneity of Wilson's Disease in Israel

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Journal Isr J Med Sci
Specialty General Medicine
Date 1977 Jan 1
PMID 838566
Citations 6
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Abstract

In a survey in Israel of 50 patients with Wilson's disease, it was found that this disease occurred in all ethnic groups. In the Arab patients there was a significantly early age of onset and the disease followed a more severe course than that in the Jewish patients. The overall sex ratio of patients was nearly 1:1, and genetic analysis of 20 families confirmed an autosomal recessive mode of inheritance. The very similar age of onset and type of disease within sibships and the varying ages of onset noted between the Arab and Jewish patients suggest that the disease is genetically heterogeneous.

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Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus.

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Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.

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