학술논문
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders
Document Type
Article
Author
Sanchis-Juan, A.; Megy, K.; Stephens, J.; Armirola Ricaurte, C.; Dewhurst, E.; Low, K.; Stirrups, K.; Erwood, M.; Penkett, C.J.; Shamardina, O.; Tuna, S.; Daugherty, L.C.; Gleadall, N.; Raymond, F.L.; Carss, K.J.; French, C.E.; Chitre, M.; Parker, A.; Woods, C.G.; Grozeva, D.; McTague, A.; Kurian, M.A.; Duarte, S.T.; Hedrera-Fernández, A.; Vogt, J.; Ambegaonkar, G.; Josifova, D.; Rankin, J.; Reid, E.; Wakeling, E.; Wassmer, E.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 3 August 2023, 110(8):1343-1355)
Subject
Language
English
ISSN
15376605
00029297
00029297