Felix B. Müller
Department of Dermatology
University of Cologne
Kerpener Str. 62
50937 Köln
Germany
Name/email consistency: high
- A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis. Müller, F.B., Huber, M., Kinaciyan, T., Hausser, I., Schaffrath, C., Krieg, T., Hohl, D., Korge, B.P., Arin, M.J. Hum. Mol. Genet. (2006)
- Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly. Müller, F.B., Küster, W., Wodecki, K., Almeida, H., Bruckner-Tuderman, L., Krieg, T., Korge, B.P., Arin, M.J. Hum. Mutat. (2006)
- A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay. Müller, F.B., Tsianakas, A., Kuwert, C., Korge, B.P., Hunzelmann, N. Br. J. Dermatol. (2005)