中华医学杂志（英文版）2018，Vol.131Issue(7)：799-803,5.DOI:10.4103/0366-6999.228245
A Novel SLC20A2 Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients
A Novel SLC20A2 Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients
Yan Ding 1Hui-Qing Dong1
作者信息
- 1. Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, China
- 折叠
摘要
关键词
Genotype/Idiopathic Basal Ganglia Calcification/Phenotype/SLC20A2Key words
Genotype/Idiopathic Basal Ganglia Calcification/Phenotype/SLC20A2引用本文复制引用
Yan Ding,Hui-Qing Dong..A Novel SLC20A2 Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients[J].中华医学杂志（英文版）,2018,131(7):799-803,5.
