SACS gene mutation
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Contents
1
Clinical significance
2
More general terms
3
Additional terms
4
References
Clinical significance
SACS
gene
mutation
are associated with:
autosomal recessive
spastic ataxia of Charlevoix-Saguenay
More general terms
gene mutation testing; gene mutation analysis
Additional terms
sacsin; DnaJ homolog subfamily C member 29; DNAJC29 (SACS, KIAA0730)
References
↑
Loinc
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