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A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

Author:

Isabelle Schrauwen,Sarah Helfmann,Akira Inagaki,Friederike Predoehl,Mohammad Amin Tabatabaiefar,Maria Magdalena Picher,Manou Sommen,Celia Zazo Seco,Jaap Oostrik,Hannie Kremer,Annelies Dheedene,Charlotte Claes,Erik Fransen et al.

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

5 October 2012

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