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Mutant VAPB: Culprit or Innocent Bystander of Amyotrophic Lateral Sclerosis?

Nearly twenty years ago a mutation in the VAPB gene, resulting in a proline to serine substitution (p.P56S), was identified as the cause of a rare, slowly progressing, familial form of the motor neuron degenerative disease Amyotrophic Lateral Sclerosis (ALS). Since then, progress in unravelling the...

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Detalles Bibliográficos
Autores principales:	Borgese, Nica, Navone, Francesca, Nukina, Nobuyuki, Yamanaka, Tomoyuki
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243577/ https://www.ncbi.nlm.nih.gov/pubmed/37366377 http://dx.doi.org/10.1177/25152564211022515

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