Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome
全外显子组测序鉴定出FAM20A基因突变是牙釉质发育不全和牙龈增生综合征的病因。
期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2011.04.005
O'Sullivan, James; Bitu, Carolina C; Daly, Sarah B; Urquhart, Jill E; Barron, Martin J; Bhaskar, Sanjeev S; Martelli-Júnior, Hercilio; dos Santos Neto, Pedro Eleuterio; Mansilla, Maria A; Murray, Jeffrey C; Coletta, Ricardo D; Black, Graeme C M; Dixon, Michael J