Small molecule drug development for rare genodermatoses – evaluation of the current status in epider...
Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa
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London: BioMed Central Ltd
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English
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London: BioMed Central Ltd
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Hereditary epidermolysis bullosa (EB) comprises a heterogeneous group of rare genodermatoses, which are caused by mutations in genes involved in the maintenance of the structural and functional integrity of dermo-epidermal adhesion in various stratified epithelia. In severe variants, generalized skin disease, extracutaneous manifestations and multi...
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Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa
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TN_cdi_doaj_primary_oai_doaj_org_article_2a582ac05c5b4cf7a645b2b2402a5186
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2a582ac05c5b4cf7a645b2b2402a5186
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ISSN
1750-1172
E-ISSN
1750-1172
DOI
10.1186/s13023-020-01467-9