Mutations in desmoglein-1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening
M.-L. Lovgren (Lead / Corresponding author), M. A. McAleer, A. D. Irvine, N. J. Wilson, S. Tavadia, M. E. Schwartz, C. Cole, A. Sandilands, F. J. D. Smith, M. Zamiri
Dive into the research topics of 'Mutations in desmoglein-1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening'. Together they form a unique fingerprint.