Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome

M. Vivero, M. T. Cho, A. Begtrup, I. M. Wentzensen, Larry Walsh, K. Payne, Y. A. Zarate, K. Bosanko, G. B. Schaefer, S. Debrosse, L. Pollack, K. Mason, K. Retterer, S. Deward, J. Juusola, W. K. Chung

Research output: Contribution to journalArticle

4 Scopus citations
Original languageEnglish (US)
JournalClinical Genetics
DOIs
StateAccepted/In press - 2017

Keywords

  • CLIFAHDD syndrome
  • de novo
  • NALCN
  • Neurodevelopmental disorder
  • Whole-exome sequencing

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Vivero, M., Cho, M. T., Begtrup, A., Wentzensen, I. M., Walsh, L., Payne, K., Zarate, Y. A., Bosanko, K., Schaefer, G. B., Debrosse, S., Pollack, L., Mason, K., Retterer, K., Deward, S., Juusola, J., & Chung, W. K. (Accepted/In press). Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Clinical Genetics. https://doi.org/10.1111/cge.12899