Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child
COX20 (FAM36A) 基因突变相关的构音障碍、共济失调和肌张力障碍：一例土耳其儿童病例报告
期刊:Annals of Indian Academy of Neurology
影响因子:1.8
doi:10.4103/aian.AIAN_536_19
Ozcanyuz, Duygu G; Incecik, Faruk; Herguner, Ozlem M; Mungan, Neslihan O; Bozdogan, Sevcan T
