A rare cause of paroxysmal movement disorder associated with TBC1D24 Gene mutation in two siblings

被引：0
|
作者：
Sarigecili, Esra [1 ]
Anlas, Ozlem [2 ]
机构：
[1] Univ Hlth Sci, Adana City Training & Res Hosp, Dept Pediat Neurol, Adana, Turkiye
[2] Univ Hlth Sci, Adana City Training & Res Hosp, Dept Med Genet, Adana, Turkiye
来源：
ANNALS OF INDIAN ACADEMY OF NEUROLOGY | 2023年 / 26卷 / 03期
关键词：
D O I：
10.4103/aian.aian_465_22
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
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页码：290 / 293
页数：4
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