Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
RUNX1 和 RUNX2 中的致病突变会产生无功能、显性负性或功能减弱的等位基因
期刊:EMBO Journal
影响因子:8.3
doi:10.1038/sj.emboj.7601568
Matheny Christina J, Speck Maren E, Cushing Patrick R, Zhou Yunpeng, Corpora Takeshi, Regan Michael, Newman Miki, Roudaia Liya, Speck Caroline L, Gu Ting-Lei, Griffey Stephen M, Bushweller John H, Speck Nancy A
