Pages that link to "Q935710"
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The following pages link to mitochondrial disease (Q935710):
Displayed 50 items.
- Mattie Stepanek (Q562894) (← links)
- sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome (Q1313757) (← links)
- Leigh disease (Q1815019) (← links)
- neuropathy, ataxia, and retinitis pigmentosa (Q3508576) (← links)
- deafness dystonia syndrome (Q3508677) (← links)
- Mitochondrial diabetes (Q4296712) (← links)
- Diabetes mellitus and deafness (Q4313947) (← links)
- coenzyme Q10 deficiency disease (Q5140809) (← links)
- GRACILE syndrome (Q5514398) (← links)
- mitochondrial myopathy (Q6881881) (← links)
- mitochondrial replacement therapy (Q7797271) (← links)
- Threshold expression (Q7798102) (← links)
- Category:Mitochondrial diseases (Q8636419) (← links)
- Pearson syndrome (Q9081107) (← links)
- ethylmalonic encephalopathy (Q17119115) (← links)
- mitochondrial DNA depletion syndrome (Q17144217) (← links)
- mitochondrial optic neuropathies (Q18390800) (← links)
- fatal infantile encephalocardiomyopathy (Q18553419) (← links)
- cytochrome-c oxidase deficiency disease (Q18556069) (← links)
- (Q18557437) (redirect page) (← links)
- combined oxidative phosphorylation deficiency (Q18987134) (← links)
- (Q19381659) (redirect page) (← links)
- Ketogenic diet in neuromuscular and neurodegenerative diseases (Q21284703) (← links)
- Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies (Q21296841) (← links)
- mitochondrial complex I deficiency (Q23542367) (← links)
- mitochondrial complex II deficiency (Q23542368) (← links)
- SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors (Q24296457) (← links)
- Unexpected vascular enrichment of SCO1 over SCO2 in mammalian tissues: implications for human mitochondrial disease (Q24300850) (← links)
- Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease (Q24302215) (← links)
- Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease (Q24308200) (← links)
- Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease (Q24313044) (← links)
- Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease (Q24336408) (← links)
- Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency (Q24337613) (← links)
- A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease (Q24533422) (← links)
- Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis (Q24630557) (← links)
- Douglass Matthew Turnbull (Q24631614) (← links)
- The microcirculation is the motor of sepsis (Q24633735) (← links)
- A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease (Q24645475) (← links)
- Bench-to-bedside review: Cytopathic hypoxia (Q24807180) (← links)
- A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation (Q26699142) (← links)
- Mitochondrial disorders in children: toward development of small-molecule treatment strategies (Q26767327) (← links)
- Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease (Q26770152) (← links)
- Mitochondrial disease in adults: what's old and what's new? (Q26776417) (← links)
- Genes and Pathways Involved in Adult Onset Disorders Featuring Muscle Mitochondrial DNA Instability (Q26801194) (← links)
- Mitochondrial diseases caused by toxic compound accumulation: from etiopathology to therapeutic approaches (Q26801561) (← links)
- Mitochondrial disease in childhood: nuclear encoded (Q26820866) (← links)
- Mitochondrial dynamism and heart disease: changing shape and shaping change (Q26825299) (← links)
- Mitochondrial complex I and cell death: a semi-automatic shotgun model (Q26829831) (← links)
- Mitochondrial genetics (Q26849285) (← links)
- Endocannabinoids in neuroendopsychology: multiphasic control of mitochondrial function (Q26852356) (← links)