Associated Papers
Novel autosomal recessive SINO syndrome-associated KIDINS220 variants provide insight into the genotype-phenotype correlation.
Yang W et al.
Heliyon, 2024
NEXMIF Combined with KIDINS220 Gene Mutation Caused Neurodevelopmental Disorder and Epilepsy: One Case Report.
Qi H et al.
Actas Espanolas De Psiquiatria, 2024
Gain-of-Function KIDINS220 Variants Disrupt Neuronal Development and Cause Cerebral Palsy.
Zhang J et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2024
Heterozygous KIDINS220/ARMS nonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity.
Josifova DJ et al.
Human Molecular Genetics, 2016
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