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A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.

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Description scientific article
Author/s

author: Angel Batuecas-Caletrio  Alvaro Gallego-Martinez  Lidia Frejo  Carmen Martín-Sierra  Teresa Requena  Jose A Lopez-Escamez  Anna Lysakowski 

Publication date June 21, 2016
Language English
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