{"title":"2个不同家族性低镁血症伴高钙尿症和肾钙沉着症家族表型和CLDN16变异体的评估:兄弟姐妹的表型差异和同卵双胞胎的表型相似性","authors":"Muhammet Akif Guler, Cigdem Yuce Kahraman","doi":"10.5152/turkjnephrol.2023.21161242","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":29873,"journal":{"name":"Turkish Journal of Nephrology","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2023-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of Phenotypes and CLDN16 Variants in 2 Different Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Families: Phenotypic Differences in Siblings and Phenotypic Similarity in Monozygotic Twins\",\"authors\":\"Muhammet Akif Guler, Cigdem Yuce Kahraman\",\"doi\":\"10.5152/turkjnephrol.2023.21161242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":29873,\"journal\":{\"name\":\"Turkish Journal of Nephrology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2023-01-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Turkish Journal of Nephrology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5152/turkjnephrol.2023.21161242\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"UROLOGY & NEPHROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Nephrology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5152/turkjnephrol.2023.21161242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
Evaluation of Phenotypes and CLDN16 Variants in 2 Different Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Families: Phenotypic Differences in Siblings and Phenotypic Similarity in Monozygotic Twins