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Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

The premutation of the fragile X messenger ribonucleoprotein 1 (FMR1) gene is characterized by an expansion of the CGG trinucleotide repeats (55 to 200 CGGs) in the 5’ untranslated region and increased levels of FMR1 mRNA. Molecular mechanisms leading to fragile X-premutation-associated conditions (...

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Detalles Bibliográficos
Autores principales: Tassone, Flora, Protic, Dragana, Allen, Emily Graves, Archibald, Alison D., Baud, Anna, Brown, Ted W., Budimirovic, Dejan B., Cohen, Jonathan, Dufour, Brett, Eiges, Rachel, Elvassore, Nicola, Gabis, Lidia V., Grudzien, Samantha J., Hall, Deborah A., Hessl, David, Hogan, Abigail, Hunter, Jessica Ezzell, Jin, Peng, Jiraanont, Poonnada, Klusek, Jessica, Kooy, R. Frank, Kraan, Claudine M., Laterza, Cecilia, Lee, Andrea, Lipworth, Karen, Losh, Molly, Loesch, Danuta, Lozano, Reymundo, Mailick, Marsha R., Manolopoulos, Apostolos, Martinez-Cerdeno, Veronica, McLennan, Yingratana, Miller, Robert M., Montanaro, Federica Alice Maria, Mosconi, Matthew W., Potter, Sarah Nelson, Raspa, Melissa, Rivera, Susan M., Shelly, Katharine, Todd, Peter K., Tutak, Katarzyna, Wang, Jun Yi, Wheeler, Anne, Winarni, Tri Indah, Zafarullah, Marwa, Hagerman, Randi J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529056/
https://www.ncbi.nlm.nih.gov/pubmed/37759552
http://dx.doi.org/10.3390/cells12182330

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