Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination
NKX6-2相关痉挛性共济失调和髓鞘发育不良的遗传和表型特征
期刊:European Journal of Neurology
影响因子:3.9
doi:10.1111/ene.14082
Chelban, V; Alsagob, M; Kloth, K; Chirita-Emandi, A; Vandrovcova, J; Maroofian, R; Davagnanam, I; Bakhtiari, S; AlSayed, M D; Rahbeeni, Z; AlZaidan, H; Malintan, N T; Johannsen, J; Efthymiou, S; Ghayoor Karimiani, E; Mankad, K; Al-Shahrani, S A; Beiraghi Toosi, M; AlShammari, M; Groppa, S; Haridy, N A; AlQuait, L; Qari, A; Huma, R; Salih, M A; Almass, R; Almutairi, F B; Hamad, M H; Alorainy, I A; Ramzan, K; Imtiaz, F; Puiu, M; Kruer, M C; Bierhals, T; Wood, N W; Colak, D; Houlden, H; Kaya, N