先天性T细胞和nk细胞免疫缺陷，中性粒细胞上β-整合素表达受损，患者KMT2D基因突变:临床病例的描述

{"title":"先天性T细胞和nk细胞免疫缺陷，中性粒细胞上β-整合素表达受损，患者KMT2D基因突变:临床病例的描述","authors":"I. Dolgopolov, E. Kochegurova, L. Grivtsova, O. K. Ustinova, M. Rykov","doi":"10.33029/0206-4952-2022-43-2-137-148","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":38750,"journal":{"name":"Immunologiya","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Congenital T- and NK-cell immunodeficiency with impaired expression of β-integrin on neutrophils in a patient with a mutation in the KMT2D gene: a description of a clinical case\",\"authors\":\"I. Dolgopolov, E. Kochegurova, L. Grivtsova, O. K. Ustinova, M. Rykov\",\"doi\":\"10.33029/0206-4952-2022-43-2-137-148\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":38750,\"journal\":{\"name\":\"Immunologiya\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Immunologiya\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.33029/0206-4952-2022-43-2-137-148\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33029/0206-4952-2022-43-2-137-148","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Immunology and Microbiology","Score":null,"Total":0}