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Study reveals diverse progression in mitochondrial DNA deletion syndromes

Summary by Medical Xpress
Researchers from the Mitochondrial Medicine Program at Children's Hospital of Philadelphia (CHOP) have better characterized a spectrum of what were classically considered discrete mitochondrial DNA deletion disease syndromes. The findings offer new insights into genetic causes, potential symptoms, and disease progression, and may inform future clinical trial development. The findings were published today in the journal Genetics in Medicine.

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Medical Xpress broke the news in on Thursday, February 20, 2025.
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