A novel de novo mutation in CSNK2A1: Reinforcing the link to neurodevelopmental abnormalities and dysmorphic features

Joanne Trinh, Irina Hüning, Nadja Budler, Volker Hingst, Katja Lohmann, Gabriele Gillessen-Kaesbach

9 Citations (Scopus)
Original languageEnglish
JournalJournal of Human Genetics
Volume62
Issue number11
Pages (from-to)1005-1006
Number of pages2
ISSN1434-5161
DOIs
Publication statusPublished - 01.11.2017

Research Areas and Centers

  • Research Area: Medical Genetics

Cite this