Associated Papers
ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration.
Yang H et al.
Molecular Genetics & Genomic Medicine, 2022
Loss-of-function variants in ARHGEF9 are associated with an X-linked intellectual disability dominant disorder.
Ghesh L et al.
Human Mutation, 2021
De novo ARHGEF9 missense variants associated with neurodevelopmental disorder in females: expanding the genotypic and phenotypic spectrum of ARHGEF9 disease in females.
Scala M et al.
Neurogenetics, 2021
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation.
Alber M et al.
Neurology. Genetics, 2017
Select a paper to view details