Publications by authors named "Maarten Van Wesemael"

1Publications

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

Authors:
Michael S Hildebrand Matías Morín Nicole C Meyer Fernando Mayo Silvia Modamio-Hoybjor Angeles Mencía Leticia Olavarrieta Carmelo Morales-Angulo Carla J Nishimura Heather Workman Adam P DeLuca Ignacio del Castillo Kyle R Taylor Bruce Tompkins Corey W Goodman Isabelle Schrauwen Maarten Van Wesemael K Lachlan A Eliot Shearer Terry A Braun Patrick L M Huygen Hannie Kremer Guy Van Camp Felipe Moreno Thomas L Casavant Richard J H Smith Miguel A Moreno-Pelayo

Hum Mutat 2011 Jul 7;32(7):825-34. Epub 2011 Jun 7.

Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City, IA 52242, USA.

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July 2011