{"title":"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。","authors":"Seyed Jalaleddin Hadei, Bardiya Ghaderi-Yazdi, Shahriar Nafissi","doi":"10.18502/cjn.v23i1.16439","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":40077,"journal":{"name":"Current Journal of Neurology","volume":"23 1","pages":"86-88"},"PeriodicalIF":0.5000,"publicationDate":"2024-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11489624/pdf/","citationCount":"0","resultStr":"{\"title\":\"Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report.\",\"authors\":\"Seyed Jalaleddin Hadei, Bardiya Ghaderi-Yazdi, Shahriar Nafissi\",\"doi\":\"10.18502/cjn.v23i1.16439\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":40077,\"journal\":{\"name\":\"Current Journal of Neurology\",\"volume\":\"23 1\",\"pages\":\"86-88\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2024-01-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11489624/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Journal of Neurology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18502/cjn.v23i1.16439\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Journal of Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/cjn.v23i1.16439","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}