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Human Molecular Genetics, 1999, Vol. 8, No. 7 1321-1328
© 1999 Oxford University Press

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families

Paul J. Couckea, Peter Van Hauwea, Philip M. Kelley1, Henricus Kunst2, Isabelle Schatteman, Désirée Van Velzen, Johan Meyers, Robbert J. Ensink2, Margriet Verstreken3, Frank Declau3, Henri Marres2, Kumar Kastury5, Shalender Bhasin5, Wyman T. McGuirt4, Richard J. H. Smith4, Cor W. R. J. Cremers2, Paul Van de Heyning3, Patrick J. Willems, Shelley D. Smith1,b and Guy Van Campb

Department of Medical Genetics, University of Antwerp–UIA, Universiteitsplein 1, 2610 Antwerp, Belgium, 1Center for Hereditary Communication Disorders, Boys Town National Research Hospital, Boys Town, NE, USA, 2Department of Otorhinolaryngology, University Hospital Nijmegen, Nijmegen, The Netherlands, 3Department of Otorhinolaryngology, University of Antwerp–UIA, Antwerp, Belgium, 4Department of Otolaryngology, University of Iowa Hospital, Iowa City, IA, USA and 5Department of Internal Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA, USA

We have previously found linkage to chromosome 1p34 in five large families with autosomal dominant non-syndromic hearing impairment (DFNA2). In all five families, the connexin31 gene (GJB3), located at 1p34 and responsible for non-syndromic autosomal dominant hearing loss in two small Chinese families, has been excluded as the responsible gene. Recently, a fourth member of the KCNQ branch of the K+ channel family, KCNQ4, has been cloned. KCNQ4 was mapped to chromosome 1p34 and a single mutation was found in three patients from a small French family with non-syndromic autosomal dominant hearing loss. In this study, we have analysed the KCNQ4 gene for mutations in our five DFNA2 families. Missense mutations altering conserved amino acids were found in three families and an inactivating deletion was present in a fourth family. No KCNQ4 mutation could be found in a single DFNA2 family of Indonesian origin. These results indicate that at least two and possibly three genes responsible for hearing impairment are located close together on chromosome 1p34 and suggest that KCNQ4 mutations may be a relatively frequent cause of autosomal dominant hearing loss.

a The first two authors contributed equally to this work

b To whom correspondence should be addressed. Tel: +323 820 2670; Fax: +323 820 2566; Email: gvcamp{at}uia.ua.ac.be


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