| 1 | SDHA, SDHAD, SDHAL |
| Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. | |
| Parfait B, Chretien D, Rotig A, Marsac C, Munnich A, Rustin P. | |
| Hum Genet 106(2):236-43. 2000 | |
| 2 | SDHA, SDHAD, SDHAL |
| Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. | |
| Bourgeron T, et al. | |
| Nat Genet 11 : 144-149. 1995 | |