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.