학술논문
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder
Document Type
Article
Author
Snijders Blok, L.; Verseput, J.; Rots, D.; Brunner, H.G.; Kleefstra, T.; den Hoed, J.; Fisher, S.E.; Venselaar, H.; Innes, A.M.; Stumpel, C.; Õunap, K.; Reinson, K.; Seaby, E.G.; McKee, S.; Burton, B.; Kim, K.; van Hagen, J.M.; Waisfisz, Q.; Joset, P.; Steindl, K.; Rauch, A.; Li, D.; Sheppard, S.E.; Hakonarson, H.; Zackai, E.H.; Keena, B.; Roos, A.; Kohlschmidt, N.; Cereda, A.; Iascone, M.; Rebessi, E.; Kernohan, K.D.; Campeau, P.M.; Millan, F.; Taylor, J.A.; Lochmüller, H.; Higgs, M.R.; Goula, A.; Bernhard, B.; Velasco, D.J.; Schmanski, A.A.; Stark, Z.; Gallacher, L.; Pais, L.; Marcogliese, P.C.; Yamamoto, S.; Raun, N.; Kramer, J.M.; Jakub, T.E.
Source
In: Human Genetics and Genomics Advances . (Human Genetics and Genomics Advances, 12 January 2023, 4(1))
Subject
Language
English
ISSN
26662477