M. Vacca, F. Filippini, A. Budillon, V. Rossi, F. D. Ragione, M. Bonis, G. Mercadante, E. Manzati, F. Gualandi, S. Bigoni, C. Trabanelli, G. Pini, E. Calzolari, A. Ferlini, I. Meloni, G. Hayek, M. Zappella, A. Renieri, M. D'urso, M. D'Esposito, F. Macdonald, A. Kerr, S. Dhanjal, M. Hultén
{"title":"《英国和意大利Rett综合征患者的MECP2基因突变分析:最常复发突变的热点图和新的MECP2保守区域的生物信息学分析》的勘误表[Brain Dev 2001;23: S246-50]","authors":"M. Vacca, F. Filippini, A. Budillon, V. Rossi, F. D. Ragione, M. Bonis, G. Mercadante, E. Manzati, F. Gualandi, S. Bigoni, C. Trabanelli, G. Pini, E. Calzolari, A. Ferlini, I. Meloni, G. Hayek, M. Zappella, A. Renieri, M. D'urso, M. D'Esposito, F. Macdonald, A. Kerr, S. Dhanjal, M. Hultén","doi":"10.1016/j.braindev.2012.09.010","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":9193,"journal":{"name":"Brain and Development","volume":"18 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]\",\"authors\":\"M. Vacca, F. Filippini, A. Budillon, V. Rossi, F. D. Ragione, M. Bonis, G. Mercadante, E. Manzati, F. Gualandi, S. Bigoni, C. Trabanelli, G. Pini, E. Calzolari, A. Ferlini, I. Meloni, G. Hayek, M. Zappella, A. Renieri, M. D'urso, M. D'Esposito, F. Macdonald, A. Kerr, S. Dhanjal, M. Hultén\",\"doi\":\"10.1016/j.braindev.2012.09.010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":9193,\"journal\":{\"name\":\"Brain and Development\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain and Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.braindev.2012.09.010\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain and Development","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.braindev.2012.09.010","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Corrigendum to “MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region” [Brain Dev 2001; 23: S246–50]