De novo missense variants inPPP1CBare associated with...

Human Genetics 2016 / 12 Vol. 135; Iss. 12

De novo missense variants inPPP1CBare associated with intellectual disability and congenital heart disease

Ma, Lijiang, Bayram, Yavuz, McLaughlin, Heather M., Cho, Megan T., Krokosky, Alyson, Turner, Clesson E., Lindstrom, Kristin, Bupp, Caleb P., Mayberry, Katey, Mu, Weiyi, Bodurtha, Joann, Weinstein, Ver
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Volume:
135
Language:
english
Journal:
Human Genetics
DOI:
10.1007/s00439-016-1731-1
Date:
December, 2016
File:
PDF, 596 KB
english, 2016
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