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.