New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish
不同种族背景的瓦尔堡微综合征患者中发现新的 RAB3GAP1 突变，丹麦可能存在创始人效应
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2010.79
Morris-Rosendahl, Deborah J; Segel, Reeval; Born, A Peter; Conrad, Christoph; Loeys, Bart; Brooks, Susan Sklower; Müller, Laura; Zeschnigk, Christine; Botti, Christina; Rabinowitz, Ron; Uyanik, Gökhan; Crocq, Marc-Antoine; Kraus, Uwe; Degen, Ingrid; Faes, Fran
