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Article

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.

European journal of human genetics : EJHG - 1 Oct 2003

Delmaghani Sedigheh, Aghaie Asadollah, Compain-Nouaille Sylvie, Ataie Afsaneh, Lemainque Arnaud, Zeinali Sirous, Lathrop Mark, Weil Dominique, Petit Christine

Abstract excerpt

We report on a novel localization for a recessive form of deafness (DFNB), by linkage analysis in an Iranian consanguineous family. Affected individuals suffer from prelingual profound sensorineural hearing loss. Genome-wide analysis led to the characterization of a new locus, DFNB40, which maps to an approximately 9 Mb interval between markers D22S427 and D22S1144 at chromosome 22q11.21-12.1. Maximum lod score...

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PMID: 14512974
DOI: 10.1038/sj.ejhg.5201045

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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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