中文

Yu Q, Shen XH, Li Y, Li RJ, Li J, Luo YY, Liu SF, Deng MY, Pei MF, Zhang GS. An intron mutation in the ACVRL1 may be associated with a transcriptional regulation defect in a Chinese family with hereditary hemorrhagic telangiectasia. PLoS One. 2013;8(2):e58031.(IF=3.73)(通讯作者

Hits:

Central South University  All rights reserved  湘ICP备05005659号-1 Click:
  MOBILE Version

The Last Update Time:..