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Article

Characterization of microsatellite markers to diagnose ADPKD.

Molecular and cellular probes - 1 Jun 2004

Bae Yoonhee, Kim Hyunho, Paik Myoah, Lee Junggeon, Hwang Daeyeon, Hwang Younghwan, Ahn Curie, Kang Seongman

Abstract excerpt

Autosomal dominant polycystic kidney disease (ADPKD) maps to chromosome 16p13.3 (PKD1) and to chromosome 4q21-23 (PKD2), with the likelihood of a third unmapped locus. The size and genomic complexity of the PKD1 gene make it impractical to detect mutations for prenatal diagnosis. Therefore, pedigree-based linkage analysis remains useful for diagnosis of ADPKD. Since, the complete genome sequences of chromosome...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15135448
DOI: 10.1016/j.mcp.2003.12.001

Genes

PKD1
PKD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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