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机译:CaCNA1a,ATP1A2和SCN1A突变在偏瘫中的贡献:芬兰偏头痛家族的临床和遗传研究
Folkhalsan Res Ctr Inst Genet Helsinki Finland;
Folkhalsan Res Ctr Inst Genet Helsinki Finland;
Univ Helsinki Cent Hosp Dept Neurol Helsinki Finland;
Univ Helsinki HiLIFE FIMM Helsinki Finland;
Folkhalsan Res Ctr Inst Genet Helsinki Finland;
Univ Helsinki Cent Hosp Dept Neurol Helsinki Finland;
Wellcome Trust Sanger Inst Wellcome Trust Genome Campus Hinxton England;
Massachusetts Gen Hosp Psychiat &
Neurodev Genet Unit Boston MA 02114 USA;
Massachusetts Gen Hosp Psychiat &
Neurodev Genet Unit Boston MA 02114 USA;
Univ Helsinki HiLIFE FIMM Helsinki Finland;
Cent Hosp Cent Finland Dept Neurol Jyvaskyla Finland;
Terveystalo Clin Res Turku Finland;
Turku Headache Ctr Turku Finland;
Terveystalo Tampere Finland;
Univ Helsinki Clin Neurosci Neurol Helsinki Finland;
Reg State Adm Agcy Northern Finland Oulu Finland;
Terveystalo Helsinki Finland;
Univ Helsinki Cent Hosp Dept Neurol Helsinki Finland;
Univ Helsinki HiLIFE FIMM Helsinki Finland;
Folkhalsan Res Ctr Inst Genet Helsinki Finland;
Univ Helsinki HiLIFE FIMM Helsinki Finland;
Univ Helsinki Cent Hosp Dept Neurol Helsinki Finland;
Migraine with aura; ICHD-3 beta criteria; clinical characteristics; ion channel; pathogenic variant; exome sequencing;
机译:CaCNA1a,ATP1A2和SCN1A突变在偏瘫中的贡献:芬兰偏头痛家族的临床和遗传研究
机译:偏瘫偏头痛中CACNA1A和ATP1A2基因的筛选:临床,遗传和功能研究
机译:筛查散发性偏瘫偏头痛患者的CACNA1A和ATP1A2突变。
机译:在体内高分辨率MRM的转基因CACNA1A敲式偏头痛小鼠模型中的自动形态学评估
机译:特征在家族性偏光中新型代谢致病机制
机译:偏瘫偏头痛中cacna1a和ATP1A2基因的筛选:临床遗传和功能研究
机译:CaCNA1a,ATP1A2和SCN1A突变在偏瘫中的贡献:芬兰偏头痛家族的临床和遗传研究