Associated Papers
A Novel EYA1 Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application.
Chen A et al.
Clinical and Experimental Otorhinolaryngology, 2023
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.
Chen A et al.
Clinical Genetics, 2021
A de novo and novel mutation in the EYA1 gene in a Chinese child with branchio-oto-renal syndrome.
Li G et al.
Intractable & Rare Diseases Research, 2018
Identification of a novel nonsynonymous mutation of EYA1 disrupting splice site in a Korean patient with BOR syndrome.
Kim HR et al.
Molecular Biology Reports, 2014
Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.
Song MH et al.
Plos One, 2013
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