Mitochondrial DNA mutations in human disease
Abstract
The human mitochondrial genome is extremely small compared with the nuclear genome, and mitochondrial genetics presents unique clinical and experimental challenges. Despite the diminutive size of the mitochondrial genome, mitochondrial DNA (mtDNA) mutations are an important cause of inherited disease. Recent years have witnessed considerable progress in understanding basic mitochondrial genetics and the relationship between inherited mutations...
Paper Details
Title
Mitochondrial DNA mutations in human disease
Published Date
May 1, 2005
Journal
Volume
6
Issue
5
Pages
389 - 402
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Notes
History