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Publications by J. Antonie Maassen
The Diabetes-Associated 3243 Mutation in the Mitochondrial tRNALeu(UUR)Gene Causes Severe Mitochondrial Dysfunction Without a Strong Decrease in Protein Synthesis Rate
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Mitochondrial tRNALeu(UUR) Mutation at Position 3243 and Symptomatic Polyneuropathy in Type 2 Diabetes
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
Hypertrophic Cardiomyopathy in Patients With Diabetes Mellitus Associated With Mitochondrial tRNALeu(UUR) Gene Mutation.
Internal Medicine
Internal Medicine
Medicine
Multiple Tumors in Mitochondrial Diabetes Associated With tRNALeu(UUR) Mutation at Position 3264
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
An 80-Year-Old Mitochondrial Disease Patient With A3243G tRNALeu(UUR) Gene Presenting Cardiac Dysfunction as the Main Symptom.
Internal Medicine
Internal Medicine
Medicine
A Case of Diabetic Amyotrophy Associated With 3243 Mitochondrial tRNA(leu; UUR) Mutation and Successful Therapy With Coenzyme Q10.
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Mitochondrial Dysfunction-Associated Arrhythmogenic Substrates in Diabetes Mellitus
Frontiers in Physiology
Physiology
Mutation in the Mitochondrial tRNAVal Causes Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Death-Associated Protein 3 Regulates Mitochondrial-Encoded Protein Synthesis and Mitochondrial Dynamics
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
