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SNCA gene mutation
Clinical significance:
- SNCA gene mutations linked to familial Parkinson's disease; Parkinson's disease 1
Related
alpha-synuclein; non-A beta component of AD amyloid; non-A4 component of amyloid; NACP (SNCA, NACP, PARK1)
General
gene mutation testing; gene mutation analysis
References
Loinc