Journal article

DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Nonsyndromic Autosomal Dominant Hearing Loss

Michael S Hildebrand, Matias Morin, Nicole C Meyer, Fernando Mayo, Silvia Modamio-Hoybjor, Angeles Mencia, 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 Show all

Human Mutation | WILEY-BLACKWELL | Published : 2011

University of Melbourne Researchers

Grants

Awarded by NIH NIDCD


Awarded by NHMRC


Awarded by NIH


Awarded by The Flemish FWO


Awarded by Spanish Ministerio de Ciencia e Innovacion


Awarded by Spanish Fondo de Investigaciones Sanitarias


Awarded by European Commission


Awarded by NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES


Awarded by NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS


Funding Acknowledgements

Contract grant sponsor: NIH NIDCD; Contract grant number: R01 (DC003544 to R.J.H.S.); Contract grant sponsor: NHMRC Overseas Biomedical Postdoctoral Training Fellowship; Contract grant number: 546493 (to M.H.); Contract grant sponsors: Doris Duke Clinical Research Fellowship (to A.S.); NIH T32; Contract grant number: GM082729 (to A.P.D.); Contract grant sponsor: The Flemish FWO; Contract grant number: G0138.07 (to G.V.C.); Contract grant sponsor: Spanish Ministerio de Ciencia e Innovacion; Contract grant number: SAF2008-03216 (to F.M.); Contract grant sponsor: Spanish Fondo de Investigaciones Sanitarias; Contract grant number: PI08/0045 (to M.A.M.P.); Contract grant sponsor: The European Commission; Contract grant number: FP6 Integrated Project: EUROHEAR, LSHG-CT-2004-512063.