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Background: Inherited epidermolysis bullosa (EB) comprises a highly heterogeneous group of rare diseases characterized by fragility and blistering of skin and mucous membranes. Clinical features combined

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To fill out medlineabstracts for references 78, individuals must provide relevant details such as the study title, authors, abstract, keywords, and publication information.

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The purpose of medlineabstracts for references 78 is to facilitate the organization and accessibility of medical research, allowing for easier reference and review by professionals in the field.

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