Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment

Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer, P. Kevin Legan, David C. Hughes, Isabelle Schatteman, Margriet Verstreken, Peter Van Hauwe, Paul Coucke, Achih Chen, Richard J.H. Smith, Thomas Somers, F. Erwin Offeciers, Paul Van De Heyning, Guy P. Richardson, Franz Wachtler, William J. Kimberling, Patrick J. Willems, Paul J. Govaerts, Guy Van Camp

Research output: Contribution to journalArticlepeer-review

294 Scopus citations

Fingerprint

Dive into the research topics of 'Mutations in the human α-tectorin gene cause autosomal dominant non- syndromic hearing impairment'. Together they form a unique fingerprint.

Medicine & Life Sciences