Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing

Overview of attention for article published in Frontiers in Genetics, January 2024

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New Research: Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing: Introduction: Inherited mitochondrial diseases are the most common group of metabolic disorders caused by a… https://t.co/

13 Jan 2024

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Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing https://t.co/R6Pd0WBkwj FrontiersinGenetics

12 Jan 2024

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