Journal Article

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

Lijiang Ma; Yavuz Bayram; Heather M. McLaughlin; Megan T. Cho; Alyson Krokosky; Clesson E. Turner; Kristin Lindstrom; Caleb P. Bupp; Katey Mayberry; Weiyi Mu; Joann Bodurtha; Veronique Weinstein; Neda Zadeh; Wendy Alcaraz; Zöe Powis; Yunru Shao; Daryl A. Scott; Andrea M. Lewis; Janson J. White; Shalani N. Jhangiani; Elif Yilmaz Gulec; Seema R. Lalani; James R. Lupski; Kyle Retterer; Rhonda E. Schnur; Ingrid M. Wentzensen; Sherri Bale; Wendy K. Chung

Human Genetics · Vol. 135, Issue 12 · pp. 1399-1409 · 2016

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Abstract

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2016-12-01
Publication Year	2016
Volume	135
Issue	12
Pages	1399-1409
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s00439-016-1731-1

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NARA Access Coverage	1964-01-01~Current
Journal Homepage	https://www.springer.com/journal/439
Publisher Page	Open Publisher Page

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