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. 2022 Nov 3;109(11):2092. doi: 10.1016/j.ajhg.2022.10.001

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability

Yan Huang, Gabrielle Lemire, Lauren C Briere, Fang Liu, Marja W Wessels, Xueqi Wang, Matthew Osmond, Oguz Kanca, Shenzhao Lu, Frances A High, Melissa A Walker, Lance H Rodan; Undiagnosed Diseases Network; Care4Rare Canada Consortium, Michael F Wangler, Shinya Yamamoto, Kristin D Kernohan, David A Sweetser, Kym M Boycott, Hugo J Bellen ∗
PMCID: PMC9674957  PMID: 36332614

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(The American Journal of Human Genetics 109, 1923–1931; October 6, 2022)

As a result of an author oversight in the originally published version of this article, Michael F. Wangler and Shinya Yamamoto were omitted from the author list. This error has now been corrected in the article online. The authors apologize for the error and any inconvenience that may have resulted.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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