A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene-Reference-Cited by-同舟云学术

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

Published:1994 Issue:6 Volume:3 Page:989-993
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Guilford Parry,Ayadi Hamadi,Blanchard Stéphane,Chaib Hassan,Paslier Denis Le,Weissenbach Jean,Drira Mohamed,Petit Christine

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/3/6/989/1608474/3-6-989.pdf

Cited by 115 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Milestones toward cochlear gene therapy for patients with hereditary hearing loss;Laryngoscope Investigative Otolaryngology;2021-08-10

3. Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future;Human Genetics;2021-07-22

4. Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges;Human Genetics;2021-07-15

5. Dual and triple AAV delivery of large therapeutic gene sequences into the inner ear;Hearing Research;2020-09

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