A novel de novo mutation in CSNK2A1 : reinforcing the link to neurodevelopmental abnormalities and dysmorphic features
JOURNAL OF HUMAN GENETICS(2017)
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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