학술논문
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling
Document Type
Article
Author
Bosakova, M.; Abraham, S.P.; Nita, A.; Svozilova, K.; Varecha, M.; Balek, L.; Krejci, P.; Hruba, E.; Buchtova, M.; Taylor, S.P.; Duran, I.; Martin, J.; Cohn, D.H.; Krakow, D.; Barta, T.; Kohoutek, J.; Radaszkiewicz, T.; Bryja, V.; Pusapati, G.V.; Rohatgi, R.; Rush, E.T.; Thiffault, I.; Nickerson, D.A.; Bamshad, M.J.
Source
In: EMBO Molecular Medicine . (EMBO Molecular Medicine, 6 November 2020, 12(11))
Subject
Language
English
ISSN
17574684
17574676
17574676