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616053.1
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Subject Details
Country
Lebanon
HPO Terms
Unsteady gait; Dysarthria; Visual impairment
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Sex
Unknown
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_001080414.4:c.5922T>G
1
Spinocerebellar Ataxia 40
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References
Jalkh et al. 2019
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