克雅二氏症(Creutzfeldt-Jakob disease)发生在一名GBA基因突变杂合子携带者身上:巧合还是后果?

I.V. Carvalho , D. Damas , I. Baldeiras , M.R. Almeida , H. Gens , G.C. Santo
{"title":"克雅二氏症(Creutzfeldt-Jakob disease)发生在一名GBA基因突变杂合子携带者身上:巧合还是后果?","authors":"I.V. Carvalho , D. Damas , I. Baldeiras , M.R. Almeida , H. Gens , G.C. Santo","doi":"10.1016/j.nrleng.2024.07.005","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":94155,"journal":{"name":"Neurologia","volume":"39 7","pages":"Pages 614-616"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2173580824000683/pdfft?md5=187a41b651794a732165a10e8f660b4a&pid=1-s2.0-S2173580824000683-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Creutzfeldt–Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence?\",\"authors\":\"I.V. Carvalho , D. Damas , I. Baldeiras , M.R. Almeida , H. Gens , G.C. Santo\",\"doi\":\"10.1016/j.nrleng.2024.07.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":94155,\"journal\":{\"name\":\"Neurologia\",\"volume\":\"39 7\",\"pages\":\"Pages 614-616\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2173580824000683/pdfft?md5=187a41b651794a732165a10e8f660b4a&pid=1-s2.0-S2173580824000683-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurologia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2173580824000683\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurologia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2173580824000683","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。
Creutzfeldt–Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence?
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
53 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信