Drosophila melanogaster as a Model to Study Fragile X-Associated Disorders

Fragile X syndrome (FXS) is a global neurodevelopmental disorder caused by the expansion of CGG trinucleotide repeats (≥200) in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene. FXS is the hallmark of Fragile X-associated disorders (FXD) and the most common monogenic cause of inherited intell...

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Detalles Bibliográficos
Autores principales: Trajković, Jelena, Makevic, Vedrana, Pesic, Milica, Pavković-Lučić, Sofija, Milojevic, Sara, Cvjetkovic, Smiljana, Hagerman, Randi, Budimirovic, Dejan B., Protic, Dragana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859539/
https://www.ncbi.nlm.nih.gov/pubmed/36672829
http://dx.doi.org/10.3390/genes14010087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859539/
https://www.ncbi.nlm.nih.gov/pubmed/36672829
http://dx.doi.org/10.3390/genes14010087

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