A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features.
Okumura A, Maruyama K, Shibata M, Kurahashi H, Ishii A, Numoto S, Hirose S, Kawai T, Iso M, Kataoka S, Okuno Y, Muramatsu H, Kojima S.
Okumura A, et al. Among authors: maruyama k.
Brain Dev. 2018 Nov;40(10):926-930. doi: 10.1016/j.braindev.2018.06.005. Epub 2018 Jun 21.
Brain Dev. 2018.
PMID: 29935962