Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

We have recently localized the gene for congenital nephrotic syndrome of the Finnish type (CNF) to chromosome 19q12-13.1. On the basis of observed recombination events, the gene was localized between markers D19S416/D19S425/D19S213/D19S208/D19S191 and D19S224. Here we have extended the mapping effor...

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Bibliografski detalji
Glavni autori: Männikkö, M, Kestailä, M, Holmberg, C, Norio, R, Ryynänen, M, Olsen, A, Peltonen, L, Tryggvason, K
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801413/
https://ncbi.nlm.nih.gov/pubmed/8533767
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