Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.

Author:

Figus A,Lampis R,Devoto M,Ristaldi M S,Ideo A,de Virgilis S,Nurchi A M,Corrias A,Corda R,Lai M E

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference11 articles.

1. I Danks DM. Hereditary disorders of copper metabolism in Wilson's disease and Menke's disease;Stanbury, J.B.,1983

2. A genetic study of Wilson's disease: evidence for heterogeneity;Cox, D.W.; Fraser, F.C.; Sass-Kortsak, A.;Am J Hum Genet,1972

3. Assignment of the gene for Wilson disease to chromosome 13: linkage to;Frydman, F.; Bonne-Tamir, B.; Farrer, L.A.,1985

4. Evidence for linkage between Wilson's disease and esterase D in three kindreds: detection of linkage for an autosomal recessive disorder by the family study method;Bonne-TamirB, Farrer L.A.; M, Frydman; H, Kanaaneh;Genet Epidemiol; Linkage of the Wilson disease gene to chromosome 13 in NorthAmerican pedigrees,1986

5. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13;Bowcock, A.M.; Farrer, L.A.; Cavalli-Sforza, L.L.;Am J Hum Genet,1987

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