{"title":"MTHFR (C677T)杂合突变继发于蛋白S缺乏和抗凝血酶III缺乏的深静脉血栓合并克罗恩病1例","authors":"Anusha Garg, Vanama Lakshman Sai, Ankit Singh, Aditi Rao","doi":"10.55691/2582-3868.1124","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":314732,"journal":{"name":"Digital Journal of Clinical Medicine","volume":"133 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Rare Case of Deep Vein Thrombosis Secondary to Protein S Deficiency and Antithrombin III Deficiency with MTHFR (C677T) Heterozygous Mutation, and Crohn’s Disease\",\"authors\":\"Anusha Garg, Vanama Lakshman Sai, Ankit Singh, Aditi Rao\",\"doi\":\"10.55691/2582-3868.1124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":314732,\"journal\":{\"name\":\"Digital Journal of Clinical Medicine\",\"volume\":\"133 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Digital Journal of Clinical Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.55691/2582-3868.1124\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Digital Journal of Clinical Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55691/2582-3868.1124","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A Rare Case of Deep Vein Thrombosis Secondary to Protein S Deficiency and Antithrombin III Deficiency with MTHFR (C677T) Heterozygous Mutation, and Crohn’s Disease