Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature

Abstract Epidermolysis Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or near the dermal-epidermal junction are mutated recessively or dominantly, and this is the primary cause of EB. Herein, two Chinese boys were diagnosed with the condition,...

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Hoofdauteurs: Fatma Mabrouk Ali (Auteur), Jieyu Zhou (Auteur), Mingyan Wang (Auteur), Qiuxia Wang (Auteur), Lulu Sun (Auteur), Mansour Maulid Mshenga (Auteur), Hongyan Lu (Auteur)
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Gepubliceerd in: BMC, 2024-04-01T00:00:00Z.
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3rd Floor Main Library

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