Associated Papers
FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9.
Piarroux J et al.
Annals of Clinical and Translational Neurology, 2020
Spinocerebellar ataxia 27 with a novel nonsense variant (Lys177X) in FGF14.
Miura S et al.
European Journal of Medical Genetics, 2019
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
Choquet K et al.
Neurogenetics, 2015
Select a paper to view details