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Updated: Feb 10, 2026

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Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing
Published on: February 10, 2023
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CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder
Josef Finsterer1, Ana C Fiorini2, Carla A Scorza3
1Krankenanstalt Rudolfstiftung, Vienna, Austria.
Abstract
No abstract available in PubMed .
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