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pro vyhledávání: '"Lakshmi V. Bugga"'
Autor:
Swati Bijlani, Ka Ming Pang, Lakshmi V. Bugga, Sampath Rangasamy, Vinodh Narayanan, Saswati Chatterjee
Publikováno v:
Frontiers in Genome Editing, Vol 6 (2024)
Rett syndrome is an acquired progressive neurodevelopmental disorder caused by de novo mutations in the X-linked MECP2 gene which encodes a pleiotropic protein that functions as a global transcriptional regulator and a chromatin modifier. Rett syndro
Externí odkaz:
https://doaj.org/article/931dac756e3a44ec9e96db46e50e069b
