Revisão Acesso aberto Revisado por pares

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

2023; Multidisciplinary Digital Publishing Institute; Volume: 12; Issue: 18 Linguagem: Inglês

10.3390/cells12182330

ISSN

2073-4409

Autores

Flora Tassone, Dragana Protić, Emily G. Allen, Alison D. Archibald, Anna Baud, Ted W. Brown, Dejan B. Budimirovic, Jonathan Cohen, Brett D. Dufour, Rachel Eiges, Nicola Elvassore, Lidia V. Gabis, Samantha J. Grudzien, Deborah A. Hall, David Hessl, Abigail L. Hogan, Jessica Ezzell Hunter, Peng Jin, Poonnada Jiraanont, Jessica Klusek, R. Frank Kooy, Claudine M. Kraan, Cecilia Laterza, Andrea Lee, Karen Lipworth, Molly Losh, Danuta Z. Loesch, Reymundo Lozano, Marsha R. Mailick, Apostolos Manolopoulos, Verónica Martínez‐Cerdeño, Yingratana McLennan, Robert M. Miller, Federica Alice Maria Montanaro, Matthew W. Mosconi, Sarah Nelson Potter, Melissa Raspa, Susan M. Rivera, Katharine E. Shelly, Peter K. Todd, Katarzyna Tutak, Jun Yi Wang, Anne Wheeler, Tri Indah Winarni, Marwa Zafarullah, Randi J. Hagerman,

Tópico(s)

Genetics and Neurodevelopmental Disorders

Resumo

The premutation of the fragile X messenger ribonucleoprotein 1 (

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