Jia Zhang, R. Cheng, Xia Yu, Zhonghui Sun, Ming Li, Z. Yao
{"title":"中国人群色素干皮病基因型和表型谱的扩展","authors":"Jia Zhang, R. Cheng, Xia Yu, Zhonghui Sun, Ming Li, Z. Yao","doi":"10.1111/phpp.12283","DOIUrl":null,"url":null,"abstract":"Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by exaggerated sunburn reactions, freckle‐like pigmentation, and a high possibility of developing cutaneous tumors. XP comprised seven complementation groups (from XP‐A to XP‐G) and a variant form XP‐V.","PeriodicalId":20060,"journal":{"name":"Photodermatology","volume":"313 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Expansion of the genotypic and phenotypic spectrum of xeroderma pigmentosum in Chinese population\",\"authors\":\"Jia Zhang, R. Cheng, Xia Yu, Zhonghui Sun, Ming Li, Z. Yao\",\"doi\":\"10.1111/phpp.12283\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by exaggerated sunburn reactions, freckle‐like pigmentation, and a high possibility of developing cutaneous tumors. XP comprised seven complementation groups (from XP‐A to XP‐G) and a variant form XP‐V.\",\"PeriodicalId\":20060,\"journal\":{\"name\":\"Photodermatology\",\"volume\":\"313 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Photodermatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1111/phpp.12283\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Photodermatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/phpp.12283","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Expansion of the genotypic and phenotypic spectrum of xeroderma pigmentosum in Chinese population
Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by exaggerated sunburn reactions, freckle‐like pigmentation, and a high possibility of developing cutaneous tumors. XP comprised seven complementation groups (from XP‐A to XP‐G) and a variant form XP‐V.