Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome
父系遗传的15q11.2微缺失证实了SNORD116 C/D盒snoRNA簇在普拉德-威利综合征中的重要作用。
期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/ejhg.2010.102
Duker, Angela L; Ballif, Blake C; Bawle, Erawati V; Person, Richard E; Mahadevan, Sangeetha; Alliman, Sarah; Thompson, Regina; Traylor, Ryan; Bejjani, Bassem A; Shaffer, Lisa G; Rosenfeld, Jill A; Lamb, Allen N; Sahoo, Trilochan