학술논문
Heterozygous HMGB1 loss-of-function variants are associated with developmental delay and microcephaly
Document Type
Article
Author
Uguen, K.; Audebert-Bellanger, S.; Redon, S.; Le Marechal, C.; Ferec, C.; Benech, C.; Krysiak, K.; Neidich, J.; Cao, Y.; Viora-Dupont, E.; Faivre, L.; Tran Mau-Them, F.; Rondeau, S.; Rio, M.; Elsharkawi, I.; Granadillo, J.L.; Soares, C.A.; Tkachenko, N.; M. Amudhavalli, S.; Engleman, K.; Boland, A.; Deleuze, J.-F.; Bezieau, S.; Odent, S.; Toutain, A.; Bonneau, D.; Gilbert-Dussardier, B.; Repnikova, E.
Source
In: Clinical Genetics . (Clinical Genetics, October 2021, 100(4):386-395)
Subject
Language
English
ISSN
13990004
00099163
00099163