Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28-Reference-Cited by-同舟云学术

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Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28

Published:2002-11-01 Issue:23 Volume:11 Page:2877-2885
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Peters L. M.

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/11/23/2877/1798458/ddf287.pdf

Cited by 90 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. Recent advances in genetic etiology of non-syndromic deafness in children;Frontiers in Neuroscience;2023-10-19

2. Grainyhead-like 2 is required for morphological integrity of mouse embryonic stem cells and orderly formation of inner ear-like organoids;Frontiers in Cell and Developmental Biology;2023-09-07

3. A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele;Human Molecular Genetics;2023-06-26

4. Clinical and genome-wide association analysis of chemoradiation-induced hearing loss in nasopharyngeal carcinoma;Human Genetics;2023-04-16

5. GRHL2 and AP2a coordinate early surface ectoderm lineage commitment during development;iScience;2023-03

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