Epidermolysis bullosa: a 2020 perspective
Author:
Affiliation:
1. The Hospital for Sick Kids 555 University Avenue Toronto ON Canada M5G 1X8
2. Department of Paediatrics University of Toronto Toronto ON Canada
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.19125
Reference6 articles.
1. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
2. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
3. Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosa
4. Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
5. Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy
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