A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease-Reference-Cited by-同舟云学术

A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease

Published:2016-06-21 Issue:16 Volume:25 Page:3407-3415
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Martín-Sierra Carmen,Requena Teresa,Frejo Lidia,Price Steven D.,Gallego-Martinez Alvaro,Batuecas-Caletrio Angel,Santos-Pérez Sofía,Soto-Varela Andrés,Lysakowski Anna,Lopez-Escamez Jose A.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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5. Meniere's disease

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