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Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome).

IF 2.5 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of Movement Disorders Pub Date : 2024-04-01 Epub Date: 2024-01-08 DOI:10.14802/jmd.23196
Jeryl Ritzi T Yu, Ruth H Walker, Adrian Danek, Connie M Westhoff, Sunitha Vege, Ilia Itin
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一名患有 XK 基因变异但没有 XK 疾病的男性出现基底神经节综合征（麦克劳德综合征）。
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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来源期刊
Journal of Movement Disorders
Journal of Movement Disorders CLINICAL NEUROLOGY-
CiteScore
2.50
自引率
5.10%
发文量
49
审稿时长
12 weeks
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