Linkage of a gene for dominant non-syndromic deafn...[Hum Mol Genet. 1995]

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1: Hum Mol Genet. 1995 Jun;4(6):1073-6. Links

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

Chen AH, Ni L, Fukushima K, Marietta J, O'Neill M, Coucke P, Willems P, Smith RJ.

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

Inherited hearing impairment can occur either in the presence of other clinical features (syndromic hearing loss, SHL) or in isolation (non-syndromic hearing loss, NSHL). The latter is more common and is highly heterogeneous. To date, six NSHL loci have been mapped. We report the identification of a seventh locus (DFNA4) on chromosome 19q13 and suggest DM kinase as a possible candidate gene.

PMID: 7655461 [PubMed - indexed for MEDLINE]

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Cited by 4 PubMed Central articles

Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
Donaudy F, Snoeckx R, Pfister M, Zenner HP, Blin N, Di Stazio M, Ferrara A, Lanzara C, Ficarella R, Declau F, et al. Am J Hum Genet. 2004 Apr; 74(4):770-6. Epub 2004 Mar 10.

[Am J Hum Genet. 2004]
A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.
Fukushima K, Kasai N, Ueki Y, Nishizaki K, Sugata K, Hirakawa S, Masuda A, Gunduz M, Ninomiya Y, Masuda Y, et al. Am J Hum Genet. 1999 Jul; 65(1):141-50.

[Am J Hum Genet. 1999]
ReviewNonsyndromic hearing impairment: unparalleled heterogeneity.
Van Camp G, Willems PJ, Smith RJ. Am J Hum Genet. 1997 Apr; 60(4):758-64.

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Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

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Cited by 4 PubMed Central articles

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