Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells
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This study was supported by the Ministry of Science and Technology of China 2014CB964803 and 2011CB811304 to JL,2012CB966704 and 2011CB66303 to FT,2014CB943104 to LW,the National Natural Science Foundation of China 31225017 and 91319310 to JL,31271543 and 31322037 to FT,the Strategic Priority Research Program of the Chinese Academy of SciencesXDA01010403,and the Shanghai Municipal Commission for Science and Technology 12JC1409600 and 13XD1404000 to JL,12JC1409400 to LW.
2015-02-06(万方平台首次上网日期,不代表论文的发表时间)
67-79