...
机译:临床表型的巴西家庭脊髓小脑的共济失调10。
Harvard Smithsonian Ctr Astrophys, SMA, Cambridge, MA 02138 USA;
Neurology Service, Federal University of Parana, Curitiba, Brazil.;
Cerebellar Ataxia; Phenotype; Nerve Tissue ProteinsSPINOCEREBELLAR ATAXIA 10MutationEpilepsyfamilySpinocerebellar Ataxia;
机译:Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
机译:Small-Expanded Allele Spinocerebellar Ataxia Type 17 Leading to Broad Movement Disorder Phenotype in a Brazilian Patient
机译:The First Korean Family of Spinocerebellar Ataxia 21 (ATX-TMEM240) with Facial Dystonic Phenotype
机译:Spinocerebellar Ataxia类型7:新摩洛哥家族的临床和遗传学研究(案例报告)
机译:Spinocerebellar Ataxia型1型蛋白质Ataxin-1用Ataxia Telanciectasia突变激酶用信号通知给DNA损伤