Mitochondrial DNA deletions and ophthalmoplegia.

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Disorders associated with multiple deletions of mitochondrial DNA.

Multiple mitochondrial DNA deletions in an elderly human individual.

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.

Increased mitochondrial DNA deletions and copy number in transfusion-dependent thalassemia.

An Investigation on Mitochondrial DNA Deletions and Telomere Shortening during Multiple Passages of Adult Stem Cells.

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.

Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes.

ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.

Recent appearance and molecular characterization of mitochondrial DNA deletions within a defined nematode pedigree.

The human immune system recognizes neopeptides derived from mitochondrial DNA deletions.

Catecholamine metabolism drives generation of mitochondrial DNA deletions in dopaminergic neurons.

Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions.

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR.

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.

Suggest Documents

Chronic progressive external ophthalmoplegia: a correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies.

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Disorders associated with multiple deletions of mitochondrial DNA.

Multiple mitochondrial DNA deletions in an elderly human individual.

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy.

Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance.

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.

Increased mitochondrial DNA deletions and copy number in transfusion-dependent thalassemia.

An Investigation on Mitochondrial DNA Deletions and Telomere Shortening during Multiple Passages of Adult Stem Cells.

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.

Mitochondrial DNA Depletion and Deletions in Paediatric Patients with Neuromuscular Diseases: Novel Phenotypes.

ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism.

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.

Recent appearance and molecular characterization of mitochondrial DNA deletions within a defined nematode pedigree.

The human immune system recognizes neopeptides derived from mitochondrial DNA deletions.

Catecholamine metabolism drives generation of mitochondrial DNA deletions in dopaminergic neurons.

Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions.

Accumulation of deletions in human mitochondrial DNA during normal aging: analysis by quantitative PCR.

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions.

Mitochondrial DNA deletions and ophthalmoplegia.

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