Literature DB >> 7655461

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

A H Chen1, L Ni, K Fukushima, J Marietta, M O'Neill, P Coucke, P Willems, R J Smith.   

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.

Entities:  

Mesh：

Substances：

Year:  1995        PMID： 7655461     DOI： 10.1093/hmg/4.6.1073

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


  16 in total

1.  A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Authors:  K Fukushima; N Kasai; Y Ueki; K Nishizaki; K Sugata; S Hirakawa; A Masuda; M Gunduz; Y Ninomiya; Y Masuda; M Sato; W T McGuirt; P Coucke; G Van Camp; R J Smith
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Myosin II regulates extension, growth and patterning in the mammalian cochlear duct.

Authors:  Norio Yamamoto; Takayuki Okano; Xuefei Ma; Robert S Adelstein; Matthew W Kelley
Journal:  Development       Date:  2009-05-13       Impact factor: 6.868

Review 3.  Deafness in the genomics era.

Authors:  A Eliot Shearer; Michael S Hildebrand; Christina M Sloan; Richard J H Smith
Journal:  Hear Res       Date:  2011-10-08       Impact factor: 3.208

4.  Molecular cloning and mapping of a novel developmentally regulated human C2H2-type zinc finger.

Authors:  K G Becker; R D Canning; J W Nagle; A M Dehejia; M H Polymeropoulos; I J Lee; A M Gado; W E Biddison; P D Drew
Journal:  Mamm Genome       Date:  1997-04       Impact factor: 2.957

Review 5.  Nonsyndromic hearing impairment: unparalleled heterogeneity.

Authors:  G Van Camp; P J Willems; R J Smith
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

6.  2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Authors:  E L Bearer; A F Chen; A H Chen; Z Li; H F Mark; R J Smith; C L Jackson
Journal:  Ann Hum Genet       Date:  2000-05       Impact factor: 1.670

7.  Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

Authors:  D A Scott; R Carmi; K Elbedour; G M Duyk; E M Stone; V C Sheffield
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

8.  Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.

Authors:  Liang Zong; Chunye Lu; Yali Zhao; Qian Li; Dongyi Han; Weiyan Yang; Yan Shen; Qingyin Zheng; Qiuju Wang
Journal:  J Genet Genomics       Date:  2012-11-16       Impact factor: 4.275

9.  Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

Authors:  Jing Zheng; Katharine K Miller; Tao Yang; Michael S Hildebrand; A Eliot Shearer; Adam P DeLuca; Todd E Scheetz; Jennifer Drummond; Steve E Scherer; P Kevin Legan; Richard J Goodyear; Guy P Richardson; Mary Ann Cheatham; Richard J Smith; Peter Dallos
Journal:  Proc Natl Acad Sci U S A       Date:  2011-02-22       Impact factor: 11.205

10.  A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.

Authors:  Michaela A H Hofrichter; Indrajit Nanda; Jens Gräf; Jörg Schröder; Wafaa Shehata-Dieler; Barbara Vona; Thomas Haaf
Journal:  Mol Syndromol       Date:  2015-09-03
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.