TY  - GEN
AU  - Renaud,Mathilde
AU  - Guissart,Claire
AU  - Mallaret,Martial
AU  - Ferdinandusse,Sacha
AU  - Cheillan,David
AU  - Drouot,Nathalie
AU  - Muller,Jean
AU  - Claustres,Mireille
AU  - Tranchant,Christine
AU  - Anheim,Mathieu
AU  - Koenig,Michel
TI  - Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia
SN  - 1432-1459
PY  - 2017///0411
KW  - Brain
KW  - diagnostic imaging
KW  - Cerebellar Ataxia
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Disability Evaluation
KW  - Disease Progression
KW  - Female
KW  - Humans
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Peroxins
KW  - Peroxisomal Disorders
KW  - blood
KW  - Receptors, Cytoplasmic and Nuclear
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1007/s00415-016-8167-3
ER  -