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
Case report: A novel mutation in the EYA1 gene in a child with branchiootic syndrome with secretory otitis media and bilateral vestibular hypofunction.
He J et al.
Frontiers in Genetics, 2023
Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta-analysis.
Chen A et al.
Clinical Genetics, 2021
EYA1 mutations leads to Branchio-Oto syndrome in two Chinese Han deaf families.
Chen P et al.
International Journal of Pediatric Otorhinolaryngology, 2019
A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndrome.
Wang YG et al.
Bmc Medical Genetics, 2018
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