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Results: 1-7 |
Results: 7
A Dutch family with progressive sensorineural hearing impairment linked tothe DFNA2 region
Authors: Ensink, RJH Huygen, PLM Van Hauwe, P Coucke, P Cremers, CWRJ Van Camp, G
Citation: Rjh. Ensink et al., A Dutch family with progressive sensorineural hearing impairment linked tothe DFNA2 region, EUR ARCH OT, 257(2), 2000, pp. 62-67
Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominanthearing loss, cluster in the channel pore region
Authors: Van Hauwe, P Coucke, PJ Ensink, RJ Huygen, P Cremers, CWRJ Van Camp, G
Citation: P. Van Hauwe et al., Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominanthearing loss, cluster in the channel pore region, AM J MED G, 93(3), 2000, pp. 184-187
DFNA 2, 5, 8, 12
Authors: Van Camp, G Coucke, PJ Van Hauwe, P Van Laer, L Verhoeven, K Wuyts, F Smith, RJH
Citation: G. Van Camp et al., DFNA 2, 5, 8, 12, ADV OTO-RH, 56, 2000, pp. 68-77
Deafness linked to DFNA2: one locus but how many genes?
Authors: Van Hauwe, P Coucke, PJ Declau, F Kunst, H Ensink, RJ Marres, HA Cremers, CWRJ Djelantik, B Smith, SD Kelley, P Van de Heyning, PH Van Camp, G
Citation: P. Van Hauwe et al., Deafness linked to DFNA2: one locus but how many genes?, NAT GENET, 21(3), 1999, pp. 263-263
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families
Authors: Coucke, PJ Van Hauwe, P Kelley, PM Kunst, H Schatteman, I Van Velzen, D Meyers, J Ensink, RJ Verstreken, M Declau, F Marres, H Kastury, K Bhasin, S McGuirt, WT Smith, RJH Cremers, CWRJ Van de Heyning, P Willems, PJ Smith, SD Van Camp, G
Citation: Pj. Coucke et al., Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families, HUM MOL GEN, 8(7), 1999, pp. 1321-1328
The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear
Authors: Van Hauwe, P Coucke, P Van Camp, G
Citation: P. Van Hauwe et al., The DFNA2 locus for hearing impairment: two genes regulating K+ ion recycling in the inner ear, BR J AUDIOL, 33(5), 1999, pp. 285-289
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome
Authors: Coucke, PJ Van Hauwe, P Everett, LA Demirhan, O Kabakkaya, Y Dietrich, NL Smith, RJH Coyle, E Reardon, W Trembath, R Willems, PJ Green, ED Van Camp, G
Citation: Pj. Coucke et al., Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome, J MED GENET, 36(6), 1999, pp. 475-477
Risultati: 1-7 |