HECW2

De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia
Esther R Berko, Megan T Cho, Christine Eng, Yunru Shao, David A Sweetser, Jessica Waxler, Nathaniel H Robin, Fallon Brewer, Sandra Donkervoort, Payam Mohassel, Carsten G Bönnemann, Martin Bialer, Christine Moore, Lynne A Wolfe, Cynthia J Tifft, Yufeng Shen, Kyle Retterer, Francisca Millan, Wendy K Chung

Journal of Medical Genetics Feb 2017, 54 (2) 84-86; DOI: 10.1136/jmedgenet-2016-103943
Mutations in HECW2 are associated with intellectual disability and epilepsy
Jonatan Halvardson, Jin J Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii-Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Soussi Zander, Ann-Charlotte Thuresson, Lars Feuk

Journal of Medical Genetics Oct 2016, 53 (10) 697-704; DOI: 10.1136/jmedgenet-2016-103814

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HECW2