Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome

D. J. Ralser, S. Kumar, O. Borisov, O. Sarig, G. Richard, S. Wolf, P. M. Krawitz, E. Sprecher, M. Kreiß, R. C. Betz*

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)756-757
Number of pages2
JournalBritish Journal of Dermatology
Volume183
Issue number4
DOIs
StatePublished - 1 Oct 2020

Cite this