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

Wilson disease (WD) is an autosomal recessively inherited disorder of copper metabolism for which the basic defect is still unknown. Twenty-seven autosomal markers were investigated for linkage in a large inbred kindred with affected individuals in two generations. Also, serum copper and ceruloplasm...

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Detaylı Bibliyografya
Asıl Yazarlar: Frydman, M, Bonné-Tamir, B, Farrer, L A, Conneally, P M, Magazanik, A, Ashbel, S, Goldwitch, Z
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1985
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC397364/
https://ncbi.nlm.nih.gov/pubmed/3856863
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