Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Fmr1-Δexon 8 rat"'
Autor:
Martina Parente, Claudia Tonini, Valeria Buzzelli, Emilia Carbone, Viviana Trezza, Valentina Pallottini
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 6; Pages: 3408
Fragile X Syndrome (FXS) is the most frequent form of inherited X-linked pathology, associated with an intellectual and developmental disability, and currently considered the first monogenic cause of autism spectrum disorder (ASD). Low levels of tota
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b17bde1d6f2c0e7210c2fd8cd1b62d03
https://hdl.handle.net/11590/401499
https://hdl.handle.net/11590/401499
Autor:
Parente M; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy., Tonini C; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy., Buzzelli V; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy., Carbone E; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy., Trezza V; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy., Pallottini V; Department of Science, Roma Tre University, Viale Marconi 446, 00146 Rome, Italy.; Neuroendocrinology Metabolism and Neuropharmacology Unit, IRCSS Fondazione Santa Lucia, Via del Fosso Fiorano 64, 00143 Rome, Italy.
Publikováno v:
International journal of molecular sciences [Int J Mol Sci] 2022 Mar 21; Vol. 23 (6). Date of Electronic Publication: 2022 Mar 21.
