TY  - GEN
AU  - Chelban,Viorica
AU  - Wiethoff,Sarah
AU  - Fabian-Jessing,Bjørn K
AU  - Haridy,Nourelhoda A
AU  - Khan,Alaa
AU  - Efthymiou,Stephanie
AU  - Becker,Esther B E
AU  - O'Connor,Emer
AU  - Hersheson,Joshua
AU  - Newland,Katrina
AU  - Hojland,Allan Thomas
AU  - Gregersen,Pernille A
AU  - Lindquist,Suzanne G
AU  - Petersen,Michael B
AU  - Nielsen,Jørgen E
AU  - Nielsen,Michael
AU  - Wood,Nicholas W
AU  - Giunti,Paola
AU  - Houlden,Henry
TI  - Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14
SN  - 1531-8257
PY  - 2019///0826
KW  - Adult
KW  - Age of Onset
KW  - Aged
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Cysteine
KW  - genetics
KW  - Disease Progression
KW  - Dystonia
KW  - etiology
KW  - Family Health
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Testing
KW  - Humans
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Peptides
KW  - Phenotype
KW  - Protein Kinase C
KW  - Spinocerebellar Ataxias
KW  - complications
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/mds.27334
ER  -