Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant

Overview of attention for article published in Frontiers in Pediatrics, May 2022

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New Research: Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant: Background The AIFM1 gene is located on chromosome Xq26.1 and encodes a flavoprotein essential for… https://t.co/bEI

04 Jul 2022

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Case Report: A Novel Intronic Mutation in AIFM1 Associated With Fatal Encephalomyopathy and Mitochondrial Disease in Infant https://t.co/gn1jaRkv4p https://t.co/3DytJIAxTd

17 Jun 2022

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