PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse-Reference-Cited by-同舟云学术

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PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

Published:1994 Issue:7 Volume:3 Page:1069-1074
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

Tassabehjl M.,Newton V. E.,Leverton K.,Turnbull K.,Seemanova E.,Kunze J.,Sperling K.,Strachan T.,Read A. P.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/3/7/1069/2446127/3-7-1069.pdf

Cited by 93 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. PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids;Biochemical and Biophysical Research Communications;2024-02

2. A gross deletion of the PAX3 gene in a large Chinese family with Waardenburg syndrome type I;World Journal of Pediatrics;2023-09-14

3. A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome;BMC Medical Genomics;2022-11-03

4. Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation;Stem Cell Research;2021-05

5. Mouse methods and models for studies in hearing;The Journal of the Acoustical Society of America;2019-11

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