Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex

1997167 citationsJournal Articlebronze Open Access

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Good health and well-being

Published in: Journal of Investigative Dermatology

Volume 108, Issue 2, pp. 220-223

Field-Weighted Citation Impact: 5.20