Mitochondrial DNA mutations in cardiomyopathy.

Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy.

Mitochondrial DNA mutations in the myelodysplastic syndrome.

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

Diseases resulting from mitochondrial DNA point mutations.

Nucleus-driven mutations of human mitochondrial DNA.

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome.

A comprehensive characterization of mitochondrial DNA mutations in glioblastoma multiforme.

Mitochondrial DNA mutations in ageing and disease: implications for HIV?

Cancer-associated isocitrate dehydrogenase mutations induce mitochondrial DNA instability.

Mitochondrial DNA exhibits resistance to induced point and deletion mutations.

Maternally transmitted mitochondrial DNA mutations can reduce lifespan.

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.

Mitochondrial Mechanisms in Septic Cardiomyopathy.

DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?

Mitochondrial DNA mutations and cognition: a case-series report.

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.

Chronic ethanol consumption increases myocardial mitochondrial DNA mutations: a potential contribution by mitochondrial topoisomerases.

Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction--reply.

Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction.

MT-CYB mutations in hypertrophic cardiomyopathy.

fusion and cardiomyopathy.

RAF1 mutations in childhood-onset dilated cardiomyopathy.

Suggest Documents

Point mutations in mitochondrial DNA in patients with hypertrophic cardiomyopathy.

Mitochondrial DNA mutations in the myelodysplastic syndrome.

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

Diseases resulting from mitochondrial DNA point mutations.

Nucleus-driven mutations of human mitochondrial DNA.

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome.

A comprehensive characterization of mitochondrial DNA mutations in glioblastoma multiforme.

Mitochondrial DNA mutations in ageing and disease: implications for HIV?

Cancer-associated isocitrate dehydrogenase mutations induce mitochondrial DNA instability.

Mitochondrial DNA exhibits resistance to induced point and deletion mutations.

Maternally transmitted mitochondrial DNA mutations can reduce lifespan.

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.

Mitochondrial Mechanisms in Septic Cardiomyopathy.

DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?

Mitochondrial DNA mutations and cognition: a case-series report.

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.

Chronic ethanol consumption increases myocardial mitochondrial DNA mutations: a potential contribution by mitochondrial topoisomerases.

Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction--reply.

Mitochondrial tRNA mutations manifest not only as hypertrophic cardiomyopathy but also as noncompaction.

MT-CYB mutations in hypertrophic cardiomyopathy.

fusion and cardiomyopathy.

RAF1 mutations in childhood-onset dilated cardiomyopathy.

Mitochondrial DNA mutations in cardiomyopathy.

Recommend Documents

Follow Us