ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.
Nanetti, Lorenzo
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. [electronic resource] - Journal of neurology Feb 2019 - 378-385 p. digital
Publication Type: Journal Article; Observational Study
1432-1459
10.1007/s00415-018-9141-z doi
Anoctamins--genetics
Cognitive Dysfunction--physiopathology
Disease Progression
Evoked Potentials, Somatosensory--physiology
Executive Function--physiology
Female
Genes, Recessive
Humans
Male
Middle Aged
Mutation
Pedigree
Spinocerebellar Ataxias--genetics
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. [electronic resource] - Journal of neurology Feb 2019 - 378-385 p. digital
Publication Type: Journal Article; Observational Study
1432-1459
10.1007/s00415-018-9141-z doi
Anoctamins--genetics
Cognitive Dysfunction--physiopathology
Disease Progression
Evoked Potentials, Somatosensory--physiology
Executive Function--physiology
Female
Genes, Recessive
Humans
Male
Middle Aged
Mutation
Pedigree
Spinocerebellar Ataxias--genetics