Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)) Elizabeth E. Palmer , Seungbeom Hong , Fatema Al Zahrani , Mais Hashem , Fajr A. Aleisa , Heba M. Jalal Ahmed , Tejaswi Kandula , Rebecca Macintosh , André E. Minoche , Clare Puttick , Velimir Gayevskiy , Alexander P. Drew , Mark J. Cowley , Marcel E. Dinger , Jill A. Rosenfeld , Rui Xiao , Megan T. Cho , Suliat F. Yakubu , Lindsay B. Henderson , Maria J. Guillen Sacoto , Amber Begtrup , Muddathir H. Hamad , Marwan Shinawi , Marisa V. Andrews , Marilyn C. Jones , Kristin Lindstrom , Ruth E. Bristol , Saima Kayani , Molly Snyder , Maria Mercedes Villanueva , Angeles Schteinschnaider , Laurence Faivre , Christel Thauvin , Antonio Vitobello , Tony Roscioli , Edwin P. Kirk , Ann M. E. Bye , Jasmeen S. Merzaban , Lukasz Jaremko , Mariusz Jaremko , Rani Sachdev , Fowzan S. Alkuraya , Stefan T. Arold American Journal of Human Genetics（2019）
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