Keyphrases
Cerebellar Atrophy
100%
Cerebellar Ataxia
100%
KIF1A
100%
Motor Domain
50%
Neurological Symptoms
33%
Neurological Disorders
33%
Arginine
16%
Histidine
16%
Brain MRI
16%
Non-motor
16%
Genetic Testing
16%
Young Female
16%
Structural Modeling
16%
Autosomal Recessive Inheritance
16%
Family History
16%
Genetic Basis
16%
Glutamine
16%
Pathogenic Variants
16%
Proline
16%
Slowly Progressive
16%
Dysarthria
16%
In Silico
16%
Population Database
16%
In Silico Tools
16%
Peptide Backbone
16%
Progressive Ataxia
16%
Gait Instability
16%
Protein Architecture
16%
Cyclic Structure
16%
Medicine and Dentistry
Cerebellar Ataxia
100%
Cerebellum Atrophy
100%
Neurologic Disease
66%
In Silico
66%
Nervous System Disorder
66%
Ataxia
33%
Family History
33%
Autosomal Dominant Inheritance
33%
Glutamine
33%
Genetic Screening
33%
Arginine
33%
Dysarthria
33%
Magnetic Resonance Imaging of Brain
33%
Histidine
33%
Proline
33%
Neuroscience
Ataxia
100%
Nervous System Disorder
66%
Arginine
33%
Histidine
33%
Magnetic Resonance Imaging of Brain
33%
Glutamine
33%
Dysarthria
33%
Proline
33%
Vertebral Column
33%
Biochemistry, Genetics and Molecular Biology
KIF1A
100%
Genetics
16%
Glutamine
16%
Autosomal Dominant Inheritance
16%
Genetic Screening
16%
Histidine
16%
Arginine
16%
Proline
16%
Magnetic Resonance Imaging
16%