A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment.

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Published in Am J Hum Genet on September 13, 2012

Authors

Isabelle Schrauwen1, 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, Morteza Hashemzadeh Chaleshtori, Paul Coucke, Amy Lee, Tobias Moser, Guy Van Camp

Author Affiliations

1: Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

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