A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant

被引:2
|
作者
Orimo, Kenta [1 ]
Kakumoto, Toshiyuki [1 ,6 ]
Hara, Ryo [1 ]
Goto, Ryoji [1 ]
Ishiura, Hiroyuki [1 ]
Mitsui, Jun [1 ,2 ]
Yoshida, Chiharu [3 ]
Uesaka, Yoshikazu [3 ]
Suzuki, Yuta [4 ]
Morishita, Shinichi [4 ]
Satake, Wataru [1 ]
Tsuji, Shoji [1 ,5 ]
Toda, Tatsushi [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Neurol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Mol Neurol, Tokyo, Japan
[3] Toranomon Gen Hosp, Dept Neurol, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol & Med Sci, Chiba, Japan
[5] Int Univ Hlth & Welf, Inst Med Genom, Narita, Chiba, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Neurol, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1138655, Japan
关键词
Primary familial brain calcification; PFBC; XPR1; Idiopathic basal ganglia calcification; IBGC; Fahr's disease; MUTATIONS;
D O I
10.1016/j.jns.2023.120732
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页数:3
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