Associated Papers
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing.
Lee WW et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2024
De novo variants in KCNJ3 are associated with early-onset epilepsy.
Li J et al.
Journal of Medical Genetics, 2024
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