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. 2019 Mar 28;104(4):778. doi: 10.1016/j.ajhg.2019.03.016

De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome

Elizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, Mais O Hashem, Fajr A Aleisa, Heba M Jalal Ahmed, Tejaswi Kandula, Rebecca Macintosh, Andre E Minoche, Clare Puttick, Velimir Gayevskiy, Alexander P Drew, Mark J Cowley, Marcel Dinger, Jill A Rosenfeld, Rui Xiao, Megan T Cho, Suliat F Yakubu, Lindsay B Henderson, Maria J Guillen Sacoto, Amber Begtrup, Muddathir Hamad, Marwan Shinawi, Marisa V Andrews, Marilyn C Jones, Kristin Lindstrom, Ruth E Bristol, Saima Kayani, Molly Snyder, Marıá Mercedes Villanueva, Angeles Schteinschnaider, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Tony Roscioli, Edwin P Kirk, Ann Bye, Jasmeen Merzaban, Łukasz Jaremko, Mariusz Jaremko, Rani K Sachdev, Fowzan S Alkuraya ∗, Stefan T Arold ∗∗
PMCID: PMC6451740  PMID: 30929740

(The American Journal of Human Genetics 104, 542–552; March 7, 2019)

In the original version of this article published on March 7, 2019, Łukasz Jaremko’s name was unfortunately misspelled as Łukas Jaremko. It appears correctly here and online. The Journal and the authors apologize for this error.

Contributor Information

Fowzan S. Alkuraya, Email: falkuraya@kfshrc.edu.sa.

Stefan T. Arold, Email: stefan.arold@kaust.edu.sa.

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

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