中文

Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract

Hits:

  • Release time:2016-07-18

  • Journal:Clin Genet.

  • Co-author:et al, Liu YL, Wang TY, Peng Y, Tong P, Guo H

  • Discipline:生物学

  • Volume:86

  • Issue:6

  • Page Number:575-579

  • Translation or Not:no

  • Date of Publication:2014-12-01

  • Links to published journals:http://www.ncbi.nlm.nih.gov/pubmed/24172257


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

The Last Update Time:..