Sign Up to like & get
recommendations!
2
Published in 2018 at "Brain"
DOI: 10.1093/brain/awy092
Abstract: Using whole exome sequencing, Fassio et al. identify de novo mutations in ATP6V1A, encoding the A subunit of v-ATPase, in four patients with developmental encephalopathies and epilepsy. Functional and expression studies demonstrate impaired lysosomal homeostasis,…
read more here.
Keywords:
mutations atp6v1a;
developmental encephalopathy;
novo mutations;
atp6v1a gene ... See more keywords