Generation of a recessive dystrophic epidermolysis bullosa mouse model with patient-derived compound heterozygous mutations
Author:
Funder
MEXT | Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Pathology and Forensic Medicine
Link
https://www.nature.com/articles/s41374-022-00735-5.pdf
Reference33 articles.
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2. Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility;Has;Br. J. Dermatol.,2020
3. Structural organization of the human type VII collagen gene (COL7A1), composed of more exons than any previously characterized gene;Christiano;Genomics,1994
4. Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes;Varki;J. Med. Genet.,2007
5. Injury- and inflammation-driven skin fibrosis: the paradigm of epidermolysis bullosa;Nystrom;Matrix Biol.,2018
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