Codice QR

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

Abstract 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 = ...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Arianna Manini, Delia Gagliardi, Megi Meneri, Sara Antognozzi, Roberto Del Bo, Cesa Scaglione, Giacomo Pietro Comi, Stefania Corti, Dario Ronchi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Wiley 2022-11-01
Serie:Annals of Clinical and Translational Neurology
Accesso online:https://doi.org/10.1002/acn3.51673
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!