Authors:
Roth, W
Deussing, J
Botchkarev, VA
Pauly-Evers, M
Saftig, P
Hafner, A
Schmidt, P
Schmahl, W
Scherer, J
Anton-Lamprecht, I
Von Figura, K
Paus, R
Peters, C
Citation: W. Roth et al., Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling, FASEB J, 14(13), 2000, pp. 2075-2086
Authors:
Muller, FB
Anton-Lamprecht, I
Kuster, W
Korge, BP
Citation: Fb. Muller et al., A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case, J INVES DER, 112(6), 1999, pp. 988-990
Authors:
Sorensen, CB
Ladekjaer-Mikkelsen, AS
Andresen, BS
Brandrup, F
Veien, NK
Buus, SK
Anton-Lamprecht, I
Kruse, TA
Jensen, PKA
Eiberg, H
Bolund, L
Gregersen, N
Citation: Cb. Sorensen et al., Identification of novel and known mutations in the genes for keratin 5 and14 in Danish patients with epidermolysis bullosa simplex: Correlation between genotype and phenotype, J INVES DER, 112(2), 1999, pp. 184-190
Authors:
Pigg, M
Gedde-Dahl, T
Cox, D
Hausser, I
Anton-Lamprecht, I
Dahl, N
Citation: M. Pigg et al., Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway, EUR J HUM G, 6(6), 1998, pp. 589-596