dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster

Fragile-X syndrome is the most common form of inherited mental retardation accompanied by other phenotypes, including macroorchidism. The disorder originates with mutations in the Fmr1 gene coding for the FMRP protein, which, with its paralogs FXR1 and FXR2, constitute a well-conserved family of RNA...

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Detalles Bibliográficos
Autores principales: Specchia, Valeria, D’Attis, Simona, Puricella, Antonietta, Bozzetti, Maria Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454977/
https://www.ncbi.nlm.nih.gov/pubmed/28509881
http://dx.doi.org/10.3390/ijms18051066

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454977/
https://www.ncbi.nlm.nih.gov/pubmed/28509881
http://dx.doi.org/10.3390/ijms18051066

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