| Literature DB >> 8298643 |
D J Peters1, L Spruit, J J Saris, D Ravine, L A Sandkuijl, R Fossdal, J Boersma, R van Eijk, S Nørby, C D Constantinou-Deltas.
Abstract
Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder. A gene defect located on the short arm of chromosome 16 is responsible for the disease in roughly 86% of affected European families. Using highly polymorphic microsatellite DNA markers, we have assigned a second gene for ADPKD to chromosome 4. In eight families with clear evidence against linkage to chromosome 16 markers, linkage analysis with the markers D4S231 and D4S423, demonstrated a multipoint lod score of 22.42.Entities:
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Year: 1993 PMID: 8298643 DOI: 10.1038/ng1293-359
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330