Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy
Andrew E. Fry(University Hospital of Wales), Seo‐Kyung Chung, Mark A. Tarnopolsky(McMaster University), Shivaram Avula(University of Liverpool), Martin A. McClatchey(Cardiff University), Anna V. Derrick(Swansea University), Sally Davies(University Hospital of Wales), Rajiv Mohanraj(Salford Royal NHS Foundation Trust), William Owen Pickrell(Swansea Bay University Health Board), Mark I. Rees(Swansea University), Lauren Brady(McMaster Children's Hospital), Yuehua Zhang(University of South China), Ying Yang(BGI Group (China)), Christopher Marra(The Graduate Center, CUNY), Ronit Mesterman(McMaster University), Adam T. Higgins(Swansea University), Johann te Water Naudé(University Hospital of Wales), Xiaodong Wang(Cipher Gene (China)), Hui Jeen Tan(Royal Manchester Children's Hospital), Denise Williams(Birmingham Women's Hospital), Kay Metcalfe(Manchester Academic Health Science Centre), Mitchell Goldfarb(The Graduate Center, CUNY)
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