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Article

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Journal of the American Society of Nephrology : JASN - 1 Jul 2003

Prakash Sunil, Chung Ki Wha, Sinha Srish, Barmada Michael, Ellis Demetrius, Ferrell Robert E, Finegold David N, Randhawa Parmjeet Singh, Dinda Amit, Vats Abhay

Abstract excerpt

Focal segmental glomerulosclerosis (FSGS) and Alport syndrome (AS) are two major causes of end-stage renal disease (ESRD). A few families with autosomal dominant FSGS have been reported with linkage to chromosome 19q13 or 11q22, while AS is usually linked to mutations in type IV collagen (COL4) s...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12819239
DOI: 10.1097/01.asn.0000071513.73427.97

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12819239-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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