Genetics

Parkinson’s Disease: LRKK2, GBA

Huntington’s Disease: HTT (trinucleotide repeat)
Alzheimer’s Disease: APP, PSEN1, PSEN2, trisomy 21, APOE-4
Multisystem Atrophy: SNCA, COQ2
Spinal muscular Atrophy: SMN1 and SMN2
Wilson’s disease: ATP7B, PRNP