Condition: NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS
rs886041715
in
GNAO1;DKFZP434H168;LOC283856
gene and
NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS
PMID 27625011
2016 Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder.
PMID 28357411
2017
GNAO1
encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
PMID 25966631
2016 Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
PMID 26060304
2016 Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation.
PMID 27068059
2016 Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.