{"title":"Recherche de la cause génétique du syndrome de Rett par l’étude du gène MECP2 chez deux patientes tunisiennes","authors":"R. Ghorbel, A. Rouissi, L. Keskes, F. Fakhfakh","doi":"10.1016/j.ando.2020.07.477","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":7881,"journal":{"name":"Annales D Endocrinologie","volume":"157 1","pages":"314"},"PeriodicalIF":0.0000,"publicationDate":"2020-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annales D Endocrinologie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.ando.2020.07.477","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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