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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Sacsin-related ataxia (ARSACS): expanding the genotype upstream from the gigantic exon
Y Ouyang1, Y Takiyama, K Sakoe
1Department of Neurology, Jichi Medical School, Tochigi 329-0498, Japan.
Neurology
|April 12, 2006
Abstract:
The authors describe a Japanese autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) patient with a compound heterozygous mutation (32627-32636delACACTGTTAC and 31760delT) in a new exon of the SACS gene. The new exons upstream of the gigantic one should be analyzed when a case is clinically compatible with ARSACS, even without any mutation in the gigantic exon.
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