Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families

Overview of attention for article published in Frontiers in Medicine, July 2024

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New Research: Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families https://t.co/OXUN4xI3i3 #FrontiersIn #Medicine

22 Aug 2024

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