Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
在小鼠模型和患有普拉德-威利综合征的人类中，印记 Ndn/NDN 等位基因沉默的随机丧失会产生功能性后果
期刊:PLoS Genetics
影响因子:3.7
doi:10.1371/journal.pgen.1003752
Rieusset Anne, Schaller Fabienne, Unmehopa Unga, Matarazzo Valery, Watrin Françoise, Linke Matthias, Georges Beatrice, Bischof Jocelyn, Dijkstra Femke, Bloemsma Monique, Corby Severine, Michel François J, Wevrick Rachel, Zechner Ulrich, Swaab Dick, Dudley Keith, Bezin Laurent, Muscatelli Françoise
