Drosophila melanogaster as a Model to Study the Multiple Phenotypes, Related to Genome Stability of the Fragile-X Syndrome

Fragile-X syndrome is one of the most common forms of inherited mental retardation and autistic behaviors. The reduction/absence of the functional FMRP protein, coded by the X-linked Fmr1 gene in humans, is responsible for the syndrome. Patients exhibit a variety of symptoms predominantly linked to...

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Bibliographische Detailangaben
Veröffentlicht in:Front Genet
Hauptverfasser: Specchia, Valeria, Puricella, Antonietta, D’Attis, Simona, Massari, Serafina, Giangrande, Angela, Bozzetti, Maria Pia
Format: Artigo
Sprache:Inglês
Veröffentlicht: Frontiers Media S.A. 2019
Schlagworte:
Genetics
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6381874/
https://ncbi.nlm.nih.gov/pubmed/30815010
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00010
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