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Autor:
Thi Thanh Huong Le, Ngoc Tung Tran, Thi Mai Lan Dao, Dinh Dung Nguyen, Huy Duong Do, Thi Lien Ha, Ralf Kühn, Thanh Liem Nguyen, Klaus Rajewsky, Van Trung Chu
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Patients with Rett syndrome (RTT) have severe mental and physical disabilities. The majority of RTT patients carry a heterozygous mutation in methyl-CpG binding protein 2 (MECP2), an X-linked gene encoding an epigenetic factor crucial for normal nerv
Externí odkaz:
https://doaj.org/article/24115b9b9c884f05a4f1cbce20d86fe4
