Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness-Reference-Cited by-同舟云学术

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Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

Published:2002-07 Issue:1 Volume:111 Page:26-30
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Ouyang Xiao,Xia Xia,Verpy Elisabeth,Du Li,Pandya Arti,Petit Christine,Balkany Thomas,Nance Walter E.,Liu Xue

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0736-0.pdf

Cited by 102 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

1. Novel heterozygous USH1C mutation impacts hair cell mechanotransduction and causes progressive hearing loss;Science Bulletin;2024-01

2. Mechanoelectrical transduction-related genetic forms of hearing loss;Current Opinion in Physiology;2023-04

3. Genomics of Dwarfism in Italian Local Chicken Breeds;Genes;2023-03-03

4. Alternative splicing in shaping the molecular landscape of the cochlea;Frontiers in Cell and Developmental Biology;2023-03-02

5. Altering gene expression using antisense oligonucleotide therapy for hearing loss;Hearing Research;2022-12

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