A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome-Reference-Cited by-同舟云学术

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A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome

Published:2003-04-24 Issue:17 Volume:348 Page:1664-1670
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Ben-Yosef Tamar,Ness Seth L.,Madeo Anne C.,Bar-Lev Adi,Wolfman Jessica H.,Ahmed Zubair M.,Desnick Robert J.,Willner Judith P.,Avraham Karen B.,Ostrer Harry,Oddoux Carole,Griffith Andrew J.,Friedman Thomas B.

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJMoa021502

Cited by 76 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. Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice;Genes;2024-06-27

2. Hearing loss;Neurogenetics for the Practitioner;2024

3. Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F;Molecular Therapy;2023-12

4. Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice;2023-09-06

5. Rescue of hearing by adenine base editing in a humanized mouse model of Usher syndrome type 1F;Molecular Therapy;2023-08

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