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注意：仅列出部分参考文献，下载原文获取全部文献信息。Cochlear Implants - Science, Serendipity, and Success
Gerard O'Donoghue
NEW ENGLAND JOURNAL OF MEDICINE (2013)
EYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner ear
Mohi Ahmed et al.
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Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families
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ORPHANET JOURNAL OF RARE DISEASES (2012)
Cilia motility and structure in primary and secondary ciliary dyskinesia
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AMERICAN JOURNAL OF RHINOLOGY & ALLERGY (2010)
The epidemiology of hearing impairment in the United States: Newborns, children, and adolescents
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OTOLARYNGOLOGY-HEAD AND NECK SURGERY (2009)
Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish
Libin Wang et al.
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A novel splice site mutation in EYA4 causes DFNA10 hearing loss
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4:: Evidence for correlation of normal cardiac phenotype mutations of the with truncating Eya domain
Tomoko Makishima et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss
J Schönberger et al.
NATURE GENETICS (2005)
Eyes absent represents a class of protein tyrosine phosphatases
JP Rayapureddi et al.
NATURE (2003)
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus
S Wayne et al.
HUMAN MOLECULAR GENETICS (2001)
Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies
N Azuma et al.
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