{"title":"印度家系新生儿Desmoglein基因5-8外显子基因缺失引起的1型局限性少毛症","authors":"Gayatri Nerakh, Sireesha, Santosh Rajeev P, Mohini Annapurna Korlimarla, A. Dalal","doi":"10.31080/aspe.2023.06.0620","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":93724,"journal":{"name":"Acta scientific paediatrics","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family\",\"authors\":\"Gayatri Nerakh, Sireesha, Santosh Rajeev P, Mohini Annapurna Korlimarla, A. Dalal\",\"doi\":\"10.31080/aspe.2023.06.0620\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":93724,\"journal\":{\"name\":\"Acta scientific paediatrics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta scientific paediatrics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31080/aspe.2023.06.0620\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta scientific paediatrics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31080/aspe.2023.06.0620","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}