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 Aug; 59(2):385-91.

[Am J Hum Genet. 1996]
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
Eur J Hum Genet. 2002 Mar; 10(3):210-2.

[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 Dec; 4(12):2391-4.

[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; 56:152-7.

[Adv Otorhinolaryngol. 2000]
ReviewNuclear and mitochondrial genes mutated in nonsyndromic impaired hearing.
Int J Pediatr Otorhinolaryngol. 2005 May; 69(5):621-47.

[Int J Pediatr Otorhinolaryngol. 2005]
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Cited by 5 PubMed Central articles

Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, et al. Am J Hum Genet. 2002 Sep; 71(3):632-6. Epub 2002 Jul 24.

[Am J Hum Genet. 2002]
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.
Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, et al. J Med Genet. 1997 Dec; 34(12):1015-7.

[J Med Genet. 1997]
ReviewNonsyndromic hearing impairment: unparalleled heterogeneity.
Van Camp G, Willems PJ, Smith RJ. Am J Hum Genet. 1997 Apr; 60(4):758-64.

[Am J Hum Genet. 1997]
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Cited by 5 PubMed Central articles

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