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Autor:
Ellery Santos, Courtney Clark, Hazel Maridith B. Biag, Si Jie Tang, Kyoungmi Kim, Matthew D. Ponzini, Andrea Schneider, Cecilia Giulivi, Federica Alice Maria Montanaro, Jesse Tran-Emilia Gipe, Jacquelyn Dayton, Jamie L. Randol, Pamela J. Yao, Apostolos Manolopoulos, Dimitrios Kapogiannis, Ye Hyun Hwang, Paul Hagerman, Randi Hagerman, Flora Tassone
Publikováno v:
Cells, Vol 12, Iss 24, p 2773 (2023)
Fragile X (FMR1) premutation is a common mutation that affects about 1 in 200 females and 1 in 450 males and can lead to the development of fragile-X-associated tremor/ataxia syndrome (FXTAS). Although there is no targeted, proven treatment for FXTAS
Externí odkaz:
https://doaj.org/article/fc408a1255164848a9edbdc8029c627d