Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort

Abstract The MFN2 gene encodes mitofusin 2, a key protein for mitochondrial fusion, transport, maintenance and cell communication. MFN2 mutations are primarily linked to Charcot–Marie–Tooth disease type 2A. However, a few cases of amyotrophic lateral sclerosis and amyotrophic lateral sclerosis/front...

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Veröffentlicht in:	Brain communications 2024-09, Vol.6 (5), p.fcae312
Hauptverfasser:	Abati, Elena, Gagliardi, Delia, Manini, Arianna, Del Bo, Roberto, Ronchi, Dario, Meneri, Megi, Beretta, Francesca, Sarno, Annalisa, Rizzo, Federica, Monfrini, Edoardo, Di Fonzo, Alessio, Pellecchia, Maria Teresa, Brusati, Alberto, Silani, Vincenzo, Comi, Giacomo Pietro, Ratti, Antonia, Verde, Federico, Ticozzi, Nicola, Corti, Stefania
Format:	Artikel
Sprache:	eng
Schlagworte:	Original
Online-Zugang:	Volltext
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