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Expanding the ataxia with oculomotor apraxia type 4 phenotype
John Reynolds
,
Malcolm Taylor
Cancer and Genomic Sciences
Research output
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Contribution to journal
›
Article
›
peer-review
22
Citations (Scopus)
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Medicine & Life Sciences
Autosomal recessive 1 Spinocerebellar ataxia
100%
Polynucleotide 5'-Hydroxyl-Kinase
64%
Phosphoric Monoester Hydrolases
41%
Phenotype
33%
Mutation
30%
Apraxias
18%
Eye Abnormalities
18%
Chorea
18%
Microcephaly
16%
Polyneuropathies
16%
Movement Disorders
15%
Eye Movements
14%
Cognitive Dysfunction
11%
Disease Progression
10%
Seizures
10%
Obesity
9%
Genes
5%