Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan-Reference-Cited by-同舟云学术

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Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan

Published:1996-01-01 Issue:1 Volume:5 Page:165-168
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Veske A.,Oehlmann R.,Younus F.,Mohyuddin A.,Muller-Myhsok B.,Qasim Mehdi S.,Gal A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/1/165/1562022/5-1-165.pdf

Reference12 articles.

1. Genes and deafness

2. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

3. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q

4. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

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2. Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre study;Journal of Otolaryngology - Head & Neck Surgery;2023-12-15

3. Deafness: from genetic architecture to gene therapy;Nature Reviews Genetics;2023-05-12

4. Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History;Audiology and Neurotology;2023

5. Molecular genetic landscape of hereditary hearing loss in Pakistan;Human Genetics;2021-07-25

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