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Publication

De Novo Mutations Affecting the Catalytic C alpha Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (vol 104, pg 139, 2019)

Journal Contribution - Journal Article

© 2019 American Society of Human Genetics (The American Journal of Human Genetics 104, 139–156; January 3, 2019) In the original version of this article published on December 27, 2018, Maura R.Z. Ruzhnikov's surname was unfortunately misspelled. It appears correctly here and online. The authors apologize for the error.
Journal: American Journal of Human Genetics
ISSN: 0002-9297
Issue: 2
Volume: 104
Pages: 357 - 357
Publication year:2019