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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

JOURNAL OF HUMAN GENETICS（2017）

Cited 24|Views27
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Abstract
A novel de novo mutation in CSNK2A1 : reinforcing the link to neurodevelopmental abnormalities and dysmorphic features
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Key words
Disease genetics,Human Genetics,Molecular Medicine,Gene Function,Gene Expression,Gene Therapy
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