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Article

A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.

European journal of human genetics : EJHG - 1 Jan 2000

Leal S M, Apaydin F, Barnwell C, Iber M, Kandogan T, Pfister M, Braendle U, Cura O, Schwalb M, Zenner H P, Vitale E

Abstract excerpt

A second kindred has been identified which supports the previously reported location of DFNB9. Linkage has been established to markers closely linked to DFNB9 which is located on 2p22-p23. The hearing impaired individuals in this highly consanguineous kindred from Eastern Turkey have prelingual profound hearing loss which affects all frequencies. A genetic map of the 2p22-p23 region where DFNB9 resides was...

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Source

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Identifiers

PMID: 9781041
DOI: 10.1038/sj.ejhg.5200201
PMCID: PMC6141006

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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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