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© Research
Publication : European journal of human genetics : EJHG

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34

Team: Auditory Therapies Innovation Lab
Member: Christine Petit
Scientific Fields
Diseases
Organisms
Applications
Technique

Published in European journal of human genetics : EJHG - 01 Mar 2002

Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C

Link to Pubmed [PMID] – 11973626

Eur. J. Hum. Genet. 2002 Mar;10(3):210-2

We report the identification of a novel locus responsible for an autosomal recessive form of hearing loss (DFNB) segregating in a Palestinian consanguineous family from Jordan. The affected individuals suffer from profound prelingual sensorineural hearing impairment. A genetic linkage with polymorphic markers surrounding D9S1776 was detected, thereby identifying a novel deafness locus, DFNB31. This locus could be assigned to a 9q32-34 region of 15 cM between markers D9S289 and D9S1881. The whirler (wi) mouse mutant, characterised by deafness and circling behaviour, maps to the corresponding region on the murine chromosome 4, thus suggesting that DFNB31 and whirler may result from orthologous gene defects.