학술논문
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
Document Type
Article
Author
Donkervoort, S.; Yun, P.; Gorokhova, S.; Geist Hauserman, J.; Hu, Y.; Uapinyoying, P.; Silverstein, S.; Bharucha-Goebel, D.; Foley, A.R.; Bolduc, V.; Bönnemann, C.G.; Krause, N.; Koliwer, J.; Ferle, P.E.; Schwake, M.; Dergai, M.; Fasshauer, D.; Cummings, B.B.; Ganesh, V.S.; Chao, K.R.; Smith, R.; Ellingwood, S.; Ghosh, P.S.; Monaghan, K.G.; Edassery, S.L.; Savas, J.N.; Snyder, M.; Iannaccone, S.T.; Dal Peraro, M.
Source
In: EMBO Molecular Medicine . (EMBO Molecular Medicine, 7 December 2021, 13(12))
Subject
Language
English
ISSN
17574684
17574676
17574676