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Article

Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.

American journal of human genetics - 1 Jul 2009

Schultz Julie M, Khan Shaheen N, Ahmed Zubair M, Riazuddin Saima, Waryah Ali M, Chhatre Dhananjay, Starost Matthew F, Ploplis Barbara, Buckley Stephanie, Velásquez David, Kabra Madhulika, Lee Kwanghyuk, Hassan Muhammad J, Ali Ghazanfar, Ansar Muhammad, Ghosh Manju, Wilcox Edward R, Ahmad Wasim, Merlino Glenn, Leal Suzanne M, Riazuddin Sheikh, Friedman Thomas B, Morell Robert J

Abstract excerpt

A gene causing autosomal-recessive, nonsyndromic hearing loss, DFNB39, was previously mapped to an 18 Mb interval on chromosome 7q11.22-q21.12. We mapped an additional 40 consanguineous families segregating nonsyndromic hearing loss to the DFNB39 locus and refined the obligate interval to 1.2 Mb....

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Identifiers

PMID: 19576567
DOI: 10.1016/j.ajhg.2009.06.003
PMCID: PMC2706959

Genes

HGF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19576567-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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