De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease

Overview of attention for article published in Human Genetics, September 2016

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PPP1CB variants associated with syndromic CHD (and Noonan spectrum features): https://t.co/2TC2nXtvGL

De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease. https://t.co/1t8IfodSZ4