Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.

Chelban, Viorica

Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14. [electronic resource] - Movement disorders : official journal of the Movement Disorder Society 07 2018 - 1119-1129 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1531-8257

10.1002/mds.27334 doi


Adult
Age of Onset
Aged
Child, Preschool
Cohort Studies
Cysteine--genetics
Disease Progression
Dystonia--etiology
Family Health
Female
Genetic Association Studies
Genetic Testing
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Mutation, Missense--genetics
Peptides--genetics
Phenotype
Protein Kinase C--genetics
Spinocerebellar Ataxias--complications
Young Adult