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Article

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.

Journal of molecular medicine (Berlin, Germany) - 1 Apr 2007

Kalay E, Caylan R, Kiroglu A F, Yasar T, Collin R W J, Heister J G A M, Oostrik J, Cremers C W R J, Brunner H G, Karaguzel A, Kremer H

Abstract excerpt

Hereditary hearing impairment is a genetically heterogeneous disorder. To date, 49 autosomal recessive nonsyndromic hearing impairment (ARNSHI) loci have been described, and there are more than 16 additional loci announced. In 25 of the known loci, causative genes have been identified. A genome scan and fine mapping revealed a novel locus for ARNSHI (DFNB63) on chromosome 11q13.2-q13.4 in a five-generation...

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Source

Identifiers

PMID: 17211611
DOI: 10.1007/s00109-006-0136-3

Genes

CTTN
FCHSD2
FGF19
FGF3
FGF4
MYEOV
TPCN2

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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A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.PMID 17211611Read ↗

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