학술논문
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
Document Type
Article
Author
Malhotra, A.; Perry, D.L.; Taft, R.; Ziegler, A.; Colin, E.; Barth, M.; Navet, B.; Rollier, P.; Bonneau, D.; Shu, L.; Xi, H.; Wang, H.; Mao, X.; Perrier, R.; Amlie-Wolf, L.; Wohler, E.; Lygia De MacEna Sobreira, N.; Vanderver, A.; Sherbini, O.; Stouffs, K.; Scalais, E.; Serretti, A.; Zhang, H.; Ferrarini, A.; Colombo, R.; Pepler, A.; Schneider, A.; Tomiwa, K.; Okamoto, N.; Matsumoto, N.; Miyake, N.
Source
In: Journal of Medical Genetics . (Journal of Medical Genetics, 1 October 2021, 58(10):712-716)
Subject
Language
English
ISSN
14686244
00222593
00222593