Literature DB >> 15958501

A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

D Yan, X Ke, S H Blanton, X M Ouyang, A Pandya, L L Du, W E Nance, X Z Liu.   

Abstract

BACKGROUND: Non-syndromic hearing loss is among the most genetically heterogeneous traits known in humans. To date, at least 50 loci for autosomal dominant non-syndromic sensorineural hearing loss (ADNSSHL) have been identified by linkage analysis.
OBJECTIVE: To report the mapping of a novel autosomal dominant deafness locus on the long arm of chromosome 14 at 14q11.2-q12, DFNA53, in a large multigenerational Chinese family with post-lingual, high frequency hearing loss that progresses to involve all frequencies.
RESULTS: A maximum multipoint LOD score of 5.4 was obtained for marker D14S1280. The analysis of recombinant haplotypes mapped DFNA53 to a 9.6 cM region interval between markers D14S581 and D14S1021. Four deafness loci (DFNA9, DFNA23, DFNB5, and DFNB35) have previously been mapped to the long arm of chromosome 14. The critical region for DFNA53 contains the gene for DFNA9 but does not overlap with the regions for DFNB5, DFNA23, or DFNB35. Screening of the COCH gene (DFNA9), BOCT, EFS, and HSPC156 within the DFNA53 interval did not identify the cause for deafness in this family.
CONCLUSIONS: Identifying the DFNA53 locus is the first step in isolating the gene responsible for hearing loss in this large multigeneration Chinese family.

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Year:  2005        PMID: 15958501      PMCID: PMC2564639          DOI: 10.1136/jmg.2005.034710

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  23 in total

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Authors:  J R O'Connell; D E Weeks
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

2.  Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics.

Authors:  E Sobel; K Lange
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3.  A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects.

Authors:  Y J de Kok; S J Bom; T M Brunt; M H Kemperman; E van Beusekom; S D van der Velde-Visser; N G Robertson; C C Morton; P L Huygen; W I Verhagen; H G Brunner; C W Cremers; F P Cremers
Journal:  Hum Mol Genet       Date:  1999-02       Impact factor: 6.150

4.  A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.

Authors:  A A Salam; F M Häfner; T E Linder; T Spillmann; A A Schinzel; S M Leal
Journal:  Am J Hum Genet       Date:  2000-04-24       Impact factor: 11.025

5.  Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan, China.

Authors:  X Z Liu; L R Xu; Y Hu; W E Nance; A Sismanis; S L Zhang; Y Xu
Journal:  Ann Otol Rhinol Laryngol       Date:  2001-04       Impact factor: 1.547

6.  Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families.

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Journal:  Hum Mutat       Date:  2001-04       Impact factor: 4.878

7.  Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.

Authors:  S J Bom; H P Kunst; P L Huygen; F P Cremers; C W Cremers
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8.  High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

Authors:  E Fransen; M Verstreken; W I Verhagen; F L Wuyts; P L Huygen; P D'Haese; N G Robertson; C C Morton; W T McGuirt; R J Smith; F Declau; P H Van de Heyning; G Van Camp
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9.  Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.

Authors:  M L Marazita; L M Ploughman; B Rawlings; E Remington; K S Arnos; W E Nance
Journal:  Am J Med Genet       Date:  1993-06-15

10.  Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction.

Authors:  N G Robertson; L Lu; S Heller; S N Merchant; R D Eavey; M McKenna; J B Nadol; R T Miyamoto; F H Linthicum; J F Lubianca Neto; A J Hudspeth; C E Seidman; C C Morton; J G Seidman
Journal:  Nat Genet       Date:  1998-11       Impact factor: 38.330

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  3 in total

Review 1.  The genetic bases for non-syndromic hearing loss among Chinese.

Authors:  Xiao Mei Ouyang; Denise Yan; Hui Jun Yuan; Dai Pu; Li Lin Du; Don Yi Han; Xue Zhong Liu
Journal:  J Hum Genet       Date:  2009-02-06       Impact factor: 3.172

2.  c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family.

Authors:  Vitor G L Dantas; Karina Lezirovitz; Guilherme L Yamamoto; Carolina Fischinger Moura de Souza; Simone Gomes Ferreira; Regina C Mingroni-Netto
Journal:  Genet Mol Biol       Date:  2014-11-14       Impact factor: 1.771

3.  Polymorphism of the 86th amino acid in CX26 protein and hereditary deafness.

Authors:  Xi Shi; Shiwei Qiu; Fendong Yan; Lizhang Shi; Yili Xuan; Wei Zhuang; Yingli Bei; Hanli Yao; Na Yuan; Shiming Yang; Yuehua Qiao
Journal:  J Otol       Date:  2016-06-10
  3 in total

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