Reply: NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness
Nicole J Van Bergen, Carole L Linster, John Christodoulou
Brain | OXFORD UNIV PRESS | Published : 2020
Awarded by Luxembourg National Research Fund (FNR)
Research aimed at developing cellular and animal models of NAD(P)HX repair disorders is supported by the Luxembourg National Research Fund (FNR) under project code C18/BM/12661133 and by a donation from the Juniclair foundation to C.L.L. Research conducted at the Murdoch Children's Research Institute (MCRI) was supported by the Victorian Government's Operational Infrastructure Support Program and the MCRI Stem Cell Medicine Pilot Project was supported by the Stafford Fox Medical Research Foundation.