Novel biallelic missense mutations in CTC1 gene identified in a Chinese family with cerebroretinal microangiopathy with calcification and cysts (CRMCC)
第一作者机构：[1]Capital Med Univ, Xuanwu Hosp, Neurol, Beijing, Peoples R China
推荐引用方式(GB/T 7714)：
Lin H..Novel biallelic missense mutations in CTC1 gene identified in a Chinese family with cerebroretinal microangiopathy with calcification and cysts (CRMCC)[J].EUROPEAN JOURNAL OF NEUROLOGY.2016,23:697-697.
APA：
Lin, H..(2016).Novel biallelic missense mutations in CTC1 gene identified in a Chinese family with cerebroretinal microangiopathy with calcification and cysts (CRMCC).EUROPEAN JOURNAL OF NEUROLOGY,23,
MLA：
Lin, H.."Novel biallelic missense mutations in CTC1 gene identified in a Chinese family with cerebroretinal microangiopathy with calcification and cysts (CRMCC)".EUROPEAN JOURNAL OF NEUROLOGY 23.(2016):697-697
