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

Verhoeven, K; Van Laer, L; Kirschhofer, K; Legan, P K; Hughes, D C; Schatteman, I; Verstreken, M; Van Hauwe, P; Coucke, P; Chen, A; Smith, R J; Somers, T; Offeciers, F E; Van de Heyning, P; Richardson, G P; Wachtler, F; Kimberling, W J; Willems, P J; Govaerts, P J; Van Camp, G

Verhoeven, K; Van Laer, L; Kirschhofer, K; Legan, P K; Hughes, D C; Schatteman, I; Verstreken, M; Van Hauwe, P; Coucke, P; Chen, A; Smith, R J; Somers, T; Offeciers, F E; Van de Heyning, P; Richardson, G P; Wachtler, F; Kimberling, W J; Willems, P J; Govaerts, P J; Van Camp, G.

Affiliation

Verhoeven K; Department of Medical Genetics, University of Antwerp (UIA), Belgium.

Nat Genet ; 19(1): 60-2, 1998 May.

Article in En | MEDLINE | ID: mdl-9590290

Subject(s)

Deafness/genetics; Extracellular Matrix Proteins/genetics; Genes, Dominant; Membrane Glycoproteins/genetics; Mutation; Alternative Splicing; Amino Acid Sequence; Animals; Base Sequence; Cosmids; DNA, Complementary; Exons; GPI-Linked Proteins; Humans; Introns; Mice; Molecular Sequence Data; Polymerase Chain Reaction; Sequence Homology, Amino Acid

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Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Extracellular Matrix Proteins / Deafness / Genes, Dominant / Mutation Limits: Animals / Humans Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1998 Document type: Article Affiliation country: Belgium Country of publication: United States

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