Epidermolysis bullosa: a 2020 perspective
- PMID: 32390183
- DOI: 10.1111/bjd.19125
Epidermolysis bullosa: a 2020 perspective
Comment on
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Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.Br J Dermatol. 2020 Oct;183(4):614-627. doi: 10.1111/bjd.18921. Epub 2020 Mar 11. Br J Dermatol. 2020. PMID: 32017015 Review.
References
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- Fine JD, Bruckner-Tuderman L, Eady RA et al. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J Am Acad Dermatol 2014; 70:1103-26.
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- Has C, Bauer JW, Bodemer C et al. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility. Br J Dermatol 2020; 183:614-27.
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- Has C, Liu L, Bolling M et al. Clinical practice guidelines for epidermolysis bullosa laboratory diagnosis. Br J Dermatol 2020; 182:574-92.
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- Lin Z, Li S, Feng C et al. Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility. Nat Genet 2016; 48:1508-16.
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- Vahidnezhad H, Youssefian L, Saeidian AH et al. Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy. Matrix Biol 2018; 66:22-33.
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