A novel missense varint in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease

Artículo original

Año: 2016

Martin-Sierra, C; Requena, T; Frejo, L; Price, SD; Gallego-Martinez, A; Batuecas-Caletrio, A; Santos-Perez, S; Soto-Varela, A; Lysakowski, A; Lopez-Escamez, JA

Título: HUMAN MOLECULAR GENETICS

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