학술논문
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephaly
Document Type
Article
Author
Herbst, C.; Bothe, V.; Wegler, M.; Abou Jamra, R.; Oppermann, H.; Axer-Schaefer, S.; Polster, T.; Audebert-Bellanger, S.; Gecz, J.; van Eyk, C.L.; Cogne, B.; Nizon, M.; Feldman, H.B.; Kurolap, A.; Horn, A.H.C.; Sticht, H.; Hurst, A.C.E.; Kelly, M.A.; Kruer, M.C.; Laquerriere, A.; Li, M.; Mark, P.R.; Morawski, M.; Stieler, J.T.; Pastinen, T.; Thifffault, I.; Saugier-Veber, P.; Vezain-Mouchard, M.; SeSong, J.; Marcorelles, P.
Source
In: Human Genetics . (Human Genetics, March 2024, 143(3):455-469)
Subject
Language
English
ISSN
14321203
03406717
03406717