Keyphrases
Ataxia
20%
ATP13A2
100%
Atrophy
20%
Autosomal Recessive
20%
Cerebellar Atrophy
20%
Cerebral Atrophy
20%
Clinical Features
20%
Consanguineous
20%
Disease Duration
40%
Disease Onset
20%
Dopamine Transporter Imaging
20%
Exon
20%
Extrapyramidal Symptoms
20%
Frameshift mutation
20%
Greenlandic Inuit
20%
Heterozygous Carrier
20%
Kufor-Rakeb Syndrome
100%
Magnetic Resonance Imaging
20%
Mutant Protein
20%
Nonsense-mediated mRNA Decay
20%
Novel mutation
100%
PARK9
100%
Parkinsonian Syndromes
20%
Pathogenic Mechanism
20%
Psychotic Features
20%
Striatum
20%
Neuroscience
Ataxia
100%
Dopamine Transporter
100%
Exon
100%
Magnetic Resonance Imaging
100%
Mutant Protein
100%
Neuropathy
100%
Parkinsonism
100%
Striatum
100%
Medicine and Dentistry
Ataxia
50%
Autosomal Recessive Inheritance
50%
Cerebral Atrophy
50%
Clinical Feature
50%
Disease Duration
100%
Diseases
50%
Dopamine Transporter
50%
Exon
50%
Heterozygote
50%
Magnetic Resonance Imaging
50%
Neuropathy
50%
Parkinsonism
50%
Striatum
50%
Biochemistry, Genetics and Molecular Biology
ATP13A2
100%
Autosomal Recessive Inheritance
20%
Dopamine Transporter
20%
Exon
20%
Genetic Carrier
20%
Heterozygote
20%
Magnetic Resonance Imaging
20%
Mutant Protein
20%
RNA
20%
Wild Type
20%
Pharmacology, Toxicology and Pharmaceutical Science
Ataxia
25%
Cerebellum Atrophy
25%
Pyramidal Sign
25%