Fatal Infantile Mitochondrial Disease With OPA1 MutationFatal Infantile Mitochondrial Disease With OPA1 Mutation

The authors establish a causal link between a pathogenic homozygous OPA1 mutation and human disease, emphasizing the vital role played by OPA1 in mitochondrial biogenesis. Journal of Medical Genetics
Source: Medscape Today Headlines - Category: Consumer Health News Tags: Pathology & Lab Medicine Journal Article Source Type: news