Authors:
Bolz, H
von Brederlow, B
Ramirez, A
Bryda, EC
Kutsche, K
Nothwang, HG
Seeliger, M
Cabrera, MDS
Vila, MC
Molina, OP
Gal, A
Kubisch, C
Citation: H. Bolz et al., Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D, NAT GENET, 27(1), 2001, pp. 108-112
Authors:
Oldenburg, J
von Brederlow, B
Fregin, A
Rost, S
Wolz, W
Eberl, W
Eber, S
Lenz, E
Schwabb, R
Brackmann, HH
Effenberger, W
Harbrecht, U
Schurgers, LJ
Vermeer, C
Muller, CR
Citation: J. Oldenburg et al., Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complex, THROMB HAEM, 84(6), 2000, pp. 937-941