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Autor:
Wei, Zhai, Hong-xiu, Hu, Liang, Le, Feng-feng, Zhuang, Ke-zhu, Wang, Ying, Zhao, Kai, Wang, Xin-min, Liu, Di’an, Sun, Xiao-ying, Wang, Shi-huan, Kuang, Ke-ping, Hu
Publikováno v:
Yi chuan = Hereditas. 38(11)
MeCP2 mutations are associated with the Rett syndrome (RTT). Currently, there is an urgent need for new animal models for RTT as the existing MeCP2 knockout mouse models fail to fully mimic the pathogenesis and symptoms of RTT patients. In order to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82849bd8db58615ed193e338644a0efa
https://pubmed.ncbi.nlm.nih.gov/27867150
https://pubmed.ncbi.nlm.nih.gov/27867150
