Journal article

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)

Funding Acknowledgements

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.