학술논문
Heterozygous variants in CTR9, which encodes a major component of the PAF1 complex, are associated with a neurodevelopmental disorder
Document Type
Article
Author
Meuwissen, M.; Verstraeten, A.; Bastiaansen, M.; Mateiu, L.; Nemegeer, M.; Meester, J.A.N.; Loeys, B.; Ranza, E.; Blanc, X.; Guerry, F.; Antonarakis, S.E.; Iwaszkiewicz, J.; Zoete, V.; Afenjar, A.; Amaral, M.; Ballhausen, D.; Barnett, S.; Barth, M.; Ziegler, A.; Asselbergh, B.; Spaas, K.; Heeman, B.; Bassetti, J.; Blackburn, P.; Schaer, M.; Casas, K.; Courtin, T.; Keren, B.; Doummar, D.; Pappas, J.; Rabin, R.; Begtrup, A.; Shinawi, M.; Vulto-van Silfhout, A.T.; Kleefstra, T.; Wagner, M.; Schaefer, E.; Gerard, B.; De Bie, C.I.; Holwerda, S.J.B.; Abbot, M.A.
Source
In: Genetics in Medicine . (Genetics in Medicine, July 2022, 24(7):1583-1591)
Subject
Language
English
ISSN
15300366
10983600
10983600