Alteration of Nucleotide Metabolism: A New Mechanism for Mitochondrial Disorders
Author:
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://www.degruyter.com/document/doi/10.1515/CCLM.2003.128/pdf
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1. Sequence and organization of the human mitochondrial genome
2. Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA
3. Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder
4. Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance
5. Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
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