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10.2147/CCID.S54681 http://scihub22266oqcxt.onion/10.2147/CCID.S54681 C4451851!4451851!26064063     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26064063&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Clin+Cosmet+Investig+Dermatol 2015 ; 8 (ä): 275-84 Nephropedia Template TP {{tp|p=26064063|t=2015. Dystrophic epidermolysis bullosa: a review |pdf=|usr=}}{{26064063}} gab.com Text Dystrophic epidermolysis bullosa: a review JO: Clin Cosmet Investig Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=26064063 #FOAvip Dystrophic epidermolysis bullosa is a rare inherited blistering disorder caused by mutations in the COL7A1 gene encoding type VII collagen. The deficiency and/or dysfunction of type VII collagen leads to subepidermal blistering immediately below the lamina densa, resulting in mucocutaneous fragility and disease complications such as intractable ulcers, extensive scarring, malnutrition, and malignancy. The disease is usually diagnosed by immunofluorescence mapping and/or transmission electron microscopy and subsequently subclassified into one of 14 subtypes. This review provides practical knowledge on the disease, including new therapeutic strategies. Twit Text FOAVip Dystrophic epidermolysis bullosa: a review ????Clin Cosmet Investig Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=26064063 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26064063 #FOAvip English Wikipedia <ref>{{Cite pmid|26064063}}</ref> Dystrophic epidermolysis bullosa: a review #MMPMID26064063 Shinkuma S Clin Cosmet Investig Dermatol 2015[]; 8 (ä): 275-84 PMID26064063show ga Dystrophic epidermolysis bullosa is a rare inherited blistering disorder caused by mutations in the COL7A1 gene encoding type VII collagen. The deficiency and/or dysfunction of type VII collagen leads to subepidermal blistering immediately below the lamina densa, resulting in mucocutaneous fragility and disease complications such as intractable ulcers, extensive scarring, malnutrition, and malignancy. The disease is usually diagnosed by immunofluorescence mapping and/or transmission electron microscopy and subsequently subclassified into one of 14 subtypes. This review provides practical knowledge on the disease, including new therapeutic strategies. äDystrophic epidermolysis bullosa: a review (epmc).pdf DeepDyve Pubget Overpricing