Associated Papers
Misdiagnosed Branchio-Oto-Renal syndrome presenting as proteinuria and renal insufficiency with insidious signs since early childhood: a report of three cases.
Lin Z et al.
Bmc Nephrology, 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 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
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