A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features.
作者信息
Trinh Joanne, Hüning Irina, Budler Nadja, Hingst Volker, Lohmann Katja, Gillessen-Kaesbach Gabriele
机构信息
Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Institut für Humangenetik, Universität zu Lübeck, Lübeck, Germany.
出版信息
J Hum Genet. 2017 Nov;62(11):1005-1006. doi: 10.1038/jhg.2017.73. Epub 2017 Jul 20.
PMID:28725024
Abstract
摘要
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