Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

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Published in Nat Genet on December 01, 1999

Authors

W T McGuirt1, S D Prasad, A J Griffith, H P Kunst, G E Green, K B Shpargel, C Runge, C Huybrechts, R F Mueller, E Lynch, M C King, H G Brunner, C W Cremers, M Takanosu, S W Li, M Arita, R Mayne, D J Prockop, G Van Camp, R J Smith

Author Affiliations

1: Molecular Otolaryngology Research Laboratories, Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City, Iowa, USA.

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