Autosomal recessive epidermolysis bullosa simplex due to BP230 deficiency (Q106957): Difference between revisions

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Forma autossômica recessiva leve de EBS devida a mutações no gene DST, que resultam na ausência do antígeno-1 do penfigoide bolhoso (BP230) nos queratinócitos basais.
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A mild autosomal recessive form of EBS due mutations in the DST gene which result in an absence of bullous pemphigoid antigen-1 (BP230) in basal keratinocytes.

Revision as of 13:57, 17 August 2026

A mild autosomal recessive form of EBS due mutations in the DST gene which result in an absence of bullous pemphigoid antigen-1 (BP230) in basal keratinocytes.
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ID_1762624893
    English
    Autosomal recessive epidermolysis bullosa simplex due to BP230 deficiency
    A mild autosomal recessive form of EBS due mutations in the DST gene which result in an absence of bullous pemphigoid antigen-1 (BP230) in basal keratinocytes.

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