Literature DB >> 19650862

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

A M Waryah1, A Rehman, Z M Ahmed, Z-H Bashir, S Y Khan, A U Zafar, S Riazuddin, T B Friedman, S Riazuddin.   

Abstract

Autosomal recessive nonsyndromic hearing impairment (ARNSHI) segregating in three unrelated, large consanguineous Pakistani families (PKDF528, PKDF859 and PKDF326) is linked to markers on chromosome 12q14.2-q15. This novel locus is designated DFNB74. Maximum two-point limit of detection (LOD) scores of 5.6, 5.7 and 2.6 were estimated for markers D12S313,D12S83 and D12S75 at theta = 0 for recessive deafness segregating in these three families. Haplotype analyses identified a critical linkage interval of 5.35 cM (5.36 Mb) defined by D12S329 at 74.58 cM and D12S313 at 79.93 cM. DFNB74 is the second ARNSHI locus mapped to chromosome 12, but the physical intervals do not overlap with one another. A locus contributing to the early onset, rapidly progressing hearing loss of A/J mice (ahl4, age-related hearing loss 4) was reported to map to chromosome 10 in a region of conserved synteny to DFNB74, suggesting that ahl4 and DFNB74 may be due to mutations of the same gene in these two species.

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Year:  2009        PMID: 19650862     DOI: 10.1111/j.1399-0004.2009.01209.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.

Authors:  Zubair M Ahmed; Rizwan Yousaf; Byung Cheon Lee; Shaheen N Khan; Sue Lee; Kwanghyuk Lee; Tayyab Husnain; Atteeq Ur Rehman; Sarah Bonneux; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal; Vadim N Gladyshev; Inna A Belyantseva; Guy Van Camp; Sheikh Riazuddin; Thomas B Friedman; Saima Riazuddin
Journal:  Am J Hum Genet       Date:  2010-12-23       Impact factor: 11.025

Review 2.  Autosomal recessive nonsyndromic deafness genes: a review.

Authors:  Duygu Duman; Mustafa Tekin
Journal:  Front Biosci (Landmark Ed)       Date:  2012-06-01

Review 3.  Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.

Authors:  Anushree Acharya; Isabelle Schrauwen; Suzanne M Leal
Journal:  Hum Genet       Date:  2021-07-22       Impact factor: 4.132

4.  Microarray analyses of otospheres derived from the cochlea in the inner ear identify putative transcription factors that regulate the characteristics of otospheres.

Authors:  Takehiro Iki; Michihiro Tanaka; Shin-Ichiro Kitajiri; Tomoko Kita; Yuri Kawasaki; Akifumi Mizukoshi; Wataru Fujibuchi; Takayuki Nakagawa; Tatsutoshi Nakahata; Juichi Ito; Koichi Omori; Megumu K Saito
Journal:  PLoS One       Date:  2017-06-29       Impact factor: 3.240

5.  Gene Therapy in Mouse Models of Deafness and Balance Dysfunction.

Authors:  Lingyan Wang; J Beth Kempton; John V Brigande
Journal:  Front Mol Neurosci       Date:  2018-08-29       Impact factor: 5.639

Review 6.  Fetal gene therapy and pharmacotherapy to treat congenital hearing loss and vestibular dysfunction.

Authors:  Michelle L Hastings; John V Brigande
Journal:  Hear Res       Date:  2020-03-05       Impact factor: 3.208

7.  Gene expression vs. sequence divergence: comparative transcriptome sequencing among natural Rhinolophus ferrumequinum populations with different acoustic phenotypes.

Authors:  Hanbo Zhao; Hui Wang; Tong Liu; Sen Liu; Longru Jin; Xiaobin Huang; Wentao Dai; Keping Sun; Jiang Feng
Journal:  Front Zool       Date:  2019-09-13       Impact factor: 3.172

  7 in total

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