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

Achih H Chen; Li Ni; Kunihiro Fukushima; Jacquie Marietta; Marsha O'Neill; Paul Coucke; Patrick Willems; Richard J H Smith

doi:10.1093/hmg/4.6.1073

Back

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

Journal article

Peer reviewed

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

Achih H Chen, Li Ni, Kunihiro Fukushima, Jacquie Marietta, Marsha O'Neill, Paul Coucke, Patrick Willems and Richard J H Smith

Human molecular genetics, Vol.4(6), pp.1073-1076

1995

DOI: 10.1093/hmg/4.6.1073

PMID: 7655461

View Online

Abstract

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.

Details

Title: Subtitle: Linkage of a gene for dominant non-syndromic deafness to chromosome 19
Creators: Achih H Chen
Li Ni
Kunihiro Fukushima
Jacquie Marietta
Marsha O'Neill
Paul Coucke
Patrick Willems
Richard J H Smith
Resource Type: Journal article
Publication Details: Human molecular genetics, Vol.4(6), pp.1073-1076
DOI: 10.1093/hmg/4.6.1073
PMID: 7655461
NLM abbreviation: Hum Mol Genet
ISSN: 0964-6906
eISSN: 1460-2083
Language: English
Date published: 1995
Academic Unit: Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
Record Identifier: 9984006442402771

Metrics

27 Record Views

66 Times Cited - Web of Science

See more details