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

D J RalserS KumarO BorisovO SarigG RichardS WolfP M KrawitzE SprecherM KreißRegina C Betz
Published in: The British journal of dermatology (2020)
Keyphrases
  • case report
  • bioinformatics analysis