Condition: Striatonigral Degeneration, Infantile, Mitochondrial
rs199476135
in
ND4;ND4L;ND3;COX3;ATP6
gene and
Striatonigral Degeneration, Infantile, Mitochondrial
PMID 7668837
1995 A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis.