Gain-of-function mutations in the ALS8 causative gene VAPB have detrimental effects on neurons and muscles

Summary Amyotrophic Lateral Sclerosis (ALS) is a motor neuron degenerative disease characterized by a progressive, and ultimately fatal, muscle paralysis. The human VAMP-Associated Protein B (hVAPB) is the causative gene of ALS type 8. Previous studies have shown that a loss-of-function mechanism is...

Full description

Bibliographic Details
Main Authors: Mario Sanhueza, Luigi Zechini, Trudy Gillespie, Giuseppa Pennetta
Format: Article
Language:English
Published: The Company of Biologists 2013-12-01
Series:Biology Open
Subjects:
Online Access:http://bio.biologists.org/content/3/1/59