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

Wilson's disease, a rare autosomal recessive disorder, has been recently mapped to the long arm of chromosome 13 (q14.1). In this study, we carried out linkage analysis between three chromosome 13 DNA markers, D13S1, D13S10, D13S2, the locus for the red cell enzyme esterase D (ESD), and the Wil...

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Bibliografiske detaljer
Main Authors: Figus, A, Lampis, R, Devoto, M, Ristaldi, M S, Ideo, A, de Virgilis, S, Nurchi, A M, Corrias, A, Corda, R, Lai, M E
Format: Artigo
Sprog:Inglês
Udgivet: 1989
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015554/
https://ncbi.nlm.nih.gov/pubmed/2563776
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