{"title":"Exome sequencing identifies ABCA7 as an important gene for familial AD cases from Eastern India","authors":"Dipanwita Sadhukhan, Adreesh Mukherjee, Bidisha Bhattacharyya, Smriti Mishra, Tapas Kumar Banerjee, Gautam Das, Uma Sinharoy, Subhra Prakash Hui, Soma Gupta, Atanu Biswas, Arindam Biswas","doi":"10.1101/2024.08.30.24312765","DOIUrl":null,"url":null,"abstract":"<strong>Introduction</strong> AD is the most complex disorder leading to dementia worldwide. Despite the disease burden among Indians the mutation spectrum in our subcontinent is not well examined.","PeriodicalId":501375,"journal":{"name":"medRxiv - Genetic and Genomic Medicine","volume":"6 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Genetic and Genomic Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.30.24312765","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction AD is the most complex disorder leading to dementia worldwide. Despite the disease burden among Indians the mutation spectrum in our subcontinent is not well examined.
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