Pages that link to "Template:Mitochondrial diseases"
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The following pages link to Template:Mitochondrial diseases:
Displayed 28 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Pearson syndrome (transclusion) (← links | edit)
- Pyruvate carboxylase deficiency (transclusion) (← links | edit)
- Friedreich's ataxia (transclusion) (← links | edit)
- Mohr–Tranebjærg syndrome (transclusion) (← links | edit)
- Category:Mitochondrial diseases (transclusion) (← links | edit)
- Chronic progressive external ophthalmoplegia (transclusion) (← links | edit)
- Diabetes and deafness (transclusion) (← links | edit)
- Kjer's optic neuropathy (transclusion) (← links | edit)
- Leber's hereditary optic neuropathy (transclusion) (← links | edit)
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (transclusion) (← links | edit)
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis (transclusion) (← links | edit)
- Neuropathy ataxia retinitis pigmentosa syndrome (transclusion) (← links | edit)
- Myoclonic epilepsy with ragged red fibers (transclusion) (← links | edit)
- Mitochondrial DNA-associated Leigh syndrome (transclusion) (← links | edit)
- Leigh syndrome, French Canadian type (transclusion) (← links | edit)
- Template:Mitochondrial enzymes (← links | edit)
- MELAS syndrome (transclusion) (← links | edit)
- Monoamine oxidase A (← links | edit)
- CHCHD10 (transclusion) (← links | edit)
- COX6B1 (transclusion) (← links | edit)
- MT-TY (transclusion) (← links | edit)
- SLC25A39 (transclusion) (← links | edit)
- UQCRB (← links | edit)
- NDUFAF2 (transclusion) (← links | edit)
- SCO1 (transclusion) (← links | edit)
- MT-TL2 (transclusion) (← links | edit)
- MERTK (transclusion) (← links | edit)
- Template:Mitochondrial proteins (← links | edit)
