Ataxia and cerebellar anomalies - narrow panelGene: KCNA1
Checked against super panel made up of the panel constituents. Ready to promote to version 1.
gene: KCNA1 was added gene: KCNA1 was added to Ataxia and cerebellar anomalies - narrow panel. Sources: Expert Review Green Mode of inheritance for gene: KCNA1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: KCNA1 were set to Episodic ataxia/myokymia syndrome,