| Literature DB >> 11701955 |
M Mrug1, W J Green, S DasGupta, D R Beier, W Lu, P D'Eustachio, L M Guay-Woodford.
Abstract
Mice homozygous for the congenital polycystic kidney (cpk) mutation develop a rapidly progressive form of polycystic kidney disease. We report an integrated genetic and physical map of the 650-kb region containing the cpk locus and the exclusion of Rrm2 and Idb2 as candidate cpk genes. Our study establishes the requisite foundation for positional cloning of the cpk gene. Copyright 2001 S. Karger AG, BaselEntities:
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Year: 2001 PMID: 11701955 DOI: 10.1159/000048783
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171