Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.

Renaud, Mathilde

Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia. [electronic resource] - Journal of neurology Aug 2016 - 1552-8 p. digital

Publication Type: Journal Article

1432-1459

10.1007/s00415-016-8167-3 doi


Brain--diagnostic imaging
Cerebellar Ataxia--genetics
DNA Mutational Analysis
Disability Evaluation
Disease Progression
Female
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Mutation, Missense--genetics
Peroxins
Peroxisomal Disorders--blood
Receptors, Cytoplasmic and Nuclear--genetics