학술논문
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders
Document Type
Article
Author
Sanchis-Juan, Alba; Megy, Karyn; Stephens, Jonathan; Armirola Ricaurte, Camila; Dewhurst, Eleanor; Low, Kayyi; French, Courtney E.; Grozeva, Detelina; Stirrups, Kathleen; Erwood, Marie; McTague, Amy; Penkett, Christopher J.; Shamardina, Olga; Tuna, Salih; Daugherty, Louise C.; Gleadall, Nicholas; Duarte, Sofia T.; Hedrera-Fernández, Antonio; Vogt, Julie; Ambegaonkar, Gautam; Chitre, Manali; Josifova, Dragana; Kurian, Manju A.; Parker, Alasdair; Rankin, Julia; Reid, Evan; Wakeling, Emma; Wassmer, Evangeline; Woods, C. Geoffrey; Raymond, F. Lucy; Carss, Keren J.
Source
In The American Journal of Human Genetics 3 August 2023 110(8):1343-1355
Subject
Language
ISSN
0002-9297