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
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
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
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