Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis

HTT full‐penetrance pathogenic repeat expansions, the genetic cause of Huntington's disease (HD), have been recently reported in a minority of frontotemporal dementia/amyotrophic lateral sclerosis (ALS) patients (0.13%). We analyzed HTT CAG repeats in an Italian cohort of ALS patients (n = 467)...

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Detalles Bibliográficos
Autores principales: Manini, Arianna, Gagliardi, Delia, Meneri, Megi, Antognozzi, Sara, Del Bo, Roberto, Scaglione, Cesa, Comi, Giacomo Pietro, Corti, Stefania, Ronchi, Dario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639631/
https://www.ncbi.nlm.nih.gov/pubmed/36285345
http://dx.doi.org/10.1002/acn3.51673

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639631/
https://www.ncbi.nlm.nih.gov/pubmed/36285345
http://dx.doi.org/10.1002/acn3.51673

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