Complex movement disorder in a patient with heterozygous YY1 mutation (Gabriele-de Vries syndrome).
Carminho-Rodrigues MT, Steel D, Sousa SB, Brandt G, Guipponi M, Laurent S, Fokstuen S, Moren A, Zacharia A, Dirren E, Oliveira R, Kurian MA, Burkhard PR, Bally JF.
Carminho-Rodrigues MT, et al. Among authors: zacharia a.
Am J Med Genet A. 2020 Sep;182(9):2129-2132. doi: 10.1002/ajmg.a.61731. Epub 2020 Jul 6.
Am J Med Genet A. 2020.
PMID: 32627382