Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome

BACKGROUND: Fragile X-associated tremor/ataxia syndrome is a late-onset neurodegenerative disorder that affects about 40% of carriers of CGG-repeat expansions in the premutation range within the fragile X gene (FMR1). Main clinical features include intention tremor, cerebellar ataxia, and parkinsoni...

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Xehetasun bibliografikoak
Argitaratua izan da:Heliyon
Egile Nagusiak: Bonapace, Giuseppe, Gullace, Rosa, Concolino, Daniela, Iannello, Grazia, Procopio, Radha, Gagliardi, Monica, Arabia, Gennarina, Barbagallo, Gaetano, Lupo, Angela, Manfredini, Lucia Ilaria, Annesi, Grazia, Quattrone, Aldo
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2019
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC6595188/
https://ncbi.nlm.nih.gov/pubmed/31294106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.heliyon.2019.e01954
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