Sign Up to like & get
recommendations!
0
Published in 2025 at "Movement Disorders Clinical Practice"
DOI: 10.1002/mdc3.70027
Abstract: Mutations in the ATP13A2 gene have been implicated in various neurodegenerative disorders, including Kufor‐Rakeb syndrome (KRS), neuronal ceroid lipofuscinosis (NCL), hereditary spastic paraplegia (HSP), and amyotrophic lateral sclerosis (ALS). This report presents two Iranian families…
read more here.
Keywords:
neuron involvement;
motor neuron;
involvement two;
two atp13a2 ... See more keywords