@article{ae50b726d79c4bf899edfba7a269a3d6,
title = "Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome",
keywords = "CLIFAHDD syndrome, de novo, NALCN, neurodevelopmental disorder, whole-exome sequencing",
author = "M. Vivero and Cho, \{M. T.\} and A. Begtrup and Wentzensen, \{I. M.\} and L. Walsh and K. Payne and Zarate, \{Y. A.\} and K. Bosanko and Schaefer, \{G. B.\} and S. DeBrosse and L. Pollack and K. Mason and K. Retterer and S. DeWard and J. Juusola and Chung, \{W. K.\}",
year = "2017",
month = jun,
doi = "10.1111/cge.12899",
language = "English",
volume = "91",
pages = "929--931",
number = "6",
}