Heterozygous frameshift mutation in keratin 5 in a family with Galli-Galli disease

A. K. Reisenauer, S. V. Wordingham, J. York, E. W. J. Kokkonen, W. H. I. McLean, N. J. Wilson, F. J. D. Smith (Lead / Corresponding author)

Research output: Contribution to journal › Article › peer-review

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Dermatology and Genetic Medicine (Strategic Grant) (Joint with Kings College London)
Barton, G. (Investigator), Campbell, P. (Investigator), Hickerson, R. (Investigator), Leigh, I. (Investigator), McLean, I. (Investigator) & Wyatt, P. (Investigator)
1/08/12 → 30/04/19
Project: Research