Medium-Chain Fatty Acids Rescue Motor Function and Neuromuscular Junction Degeneration in a <i>Drosophila</i> Model of Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease characterised by progressive degeneration of the motor neurones. An expanded <i>GGGGCC (G4C2)</i> hexanucleotide repeat in <i>C9orf72</i> is the most common genetic cause of ALS and frontotemporal dementia (FTD); therefo...

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Detalhes bibliográficos

Principais autores:	Ella Dunn, Joern R. Steinert, Aelfwin Stone, Virender Sahota, Robin S. B. Williams, Stuart Snowden, Hrvoje Augustin
Formato:	Artigo
Idioma:	Inglês
Publicado em:	MDPI AG 2023-08-01
Colecção:	Cells
Assuntos:	ALS MCFA 4-MOA NA <i>Drosophila</i> motor function
Acesso em linha:	https://www.mdpi.com/2073-4409/12/17/2163
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