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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 epider...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2a582ac05c5b4cf7a645b2b2402a5186

Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa

About this item

Full title

Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa

Publisher

London: BioMed Central Ltd

Journal title

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-292, Article 292

Language

English

Formats

Publication information

Publisher

London: BioMed Central Ltd

More information

Scope and Contents

Contents

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...

Alternative Titles

Full title

Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2a582ac05c5b4cf7a645b2b2402a5186

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2a582ac05c5b4cf7a645b2b2402a5186

Other Identifiers

ISSN

1750-1172

E-ISSN

1750-1172

DOI

10.1186/s13023-020-01467-9

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