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Autor:
Hayes Wong, Alexander W.M. Hooper, Hye Ri Kang, Shiron J. Lee, Jiayi Zhao, Chanchal Sadhu, Satinder Rawat, Steven J. Gray, David R. Hampson
Publikováno v:
JCI Insight, Vol 8, Iss 11 (2023)
Fragile X syndrome is a neurodevelopmental disorder caused by the absence of the mRNA-binding protein fragile X messenger ribonucleoprotein (FMRP). Because FMRP is a highly pleiotropic protein controlling the expression of hundreds of genes, viral ve
Externí odkaz:
https://doaj.org/article/7f55ad7e4b43445b8fa490f3c56b476a