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Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report.

IF 0.5 Q4 CLINICAL NEUROLOGY
Current Journal of Neurology Pub Date : 2024-01-05 DOI:10.18502/cjn.v23i1.16439
Seyed Jalaleddin Hadei, Bardiya Ghaderi-Yazdi, Shahriar Nafissi
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一名伊朗患者因罕见的 VPS13A 基因突变导致长期亚临床重度高钾血症：病例报告。
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
Current Journal of Neurology
Current Journal of Neurology CLINICAL NEUROLOGY-
CiteScore
0.80
自引率
14.30%
发文量
30
审稿时长
12 weeks
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