EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts withSIX3both physically and functionally-Reference-Cited by-同舟云学术

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EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts withSIX3both physically and functionally

Published:2009-10 Issue:10 Volume:30 Page:E946-E955
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Abe Yuichi,Oka Akira,Mizuguchi Masashi,Igarashi Takashi,Ishikawa Shumpei,Aburatani Hiroyuki,Yokoyama Shigetoshi,Asahara Hiroshi,Nagao Kazuaki,Yamada Masao,Miyashita Toshiyuki

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21094/fullpdf

Cited by 24 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. Identification of a novel mutation of EYA4 in a Chinese family with delayed nonsyndromic hearing loss and analysis of molecular epidemiology of EYA4 mutations;2024-03-25

2. Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss;BMC Medical Genomics;2022-05-16

3. Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants;Scientific Reports;2020-04-10

4. Prevalence and clinical features of hearing loss caused by EYA4 variants;Scientific Reports;2020-02-27

5. Midline Patterning Defects;Developmental Neuropathology;2018-03-09

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