An autosomal recessive nonsyndromic form of sensor...[Genome Res. 1995]

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1: Genome Res. 1995 Oct;5(3):305-8. Links

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER, Smith SD, Kenyon JB, Zbar RI, Smith RJ.

Department of Otolaryngology, University of Iowa, Iowa City 52242, USA.

Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of congenitally acquired inherited hearing impairment. Although numerous loci are believed to exist, only five have been identified. Using a pooled genomic DNA screening strategy, we have identified a sixth locus, DFNB6, on 3p in the interval bounded by D3S1619 and D3S1766.

PMID: 8593615 [PubMed - indexed for MEDLINE]

An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds. [Am J Hum Genet. 1996]
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34. [Eur J Hum Genet. 2002]
A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus. [Hum Mol Genet. 1995]
ReviewSensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss. [Adv Otorhinolaryngol. 2000]
ReviewNuclear and mitochondrial genes mutated in nonsyndromic impaired hearing. [Int J Pediatr Otorhinolaryngol. 2005]

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An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

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