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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Figus, A, Lampis, R, Devoto, M, Ristaldi, M S, Ideo, A, de Virgilis, S, Nurchi, A M, Corrias, A, Corda, R, Lai, M E
Médium: Artigo
Jazyk:Inglês
Vydáno: 1989
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015554/
https://ncbi.nlm.nih.gov/pubmed/2563776
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky