Hereditary defect of cobalamin metabolism with adolescence onset resembling multiple sclerosis: 41-year follow up in two cases
两例青少年期发病、类似多发性硬化症的遗传性钴胺素代谢缺陷：41年随访
期刊:Therapeutic Advances in Neurological Disorders
影响因子:4.1
doi:10.1177/1756286419872115
Motte, Jeremias; Kneiphof, Janina; Straßburger-Krogias, Katrin; Pitarokoili, Kalliopi; Fisse, Anna Lena; Kappos, Ludwig; Gold, Ralf
