Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome

Overview of attention for article published in Frontiers in Genetics, January 2020

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https://t.co/77MCD3xZkF

11 Feb 2020

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New Research: Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome: Encephalomyopathic mitochondrial DNA (mtDNA) depletion syndrome 13 (MTDPS13) is a rare genetic disorder caused by defects in F-box… https://t.co/NnDw

09 Jan 2020

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