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Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 11/2016, Volume 136, Issue 11, pp. 2119 - 2121
Epidermolysis bullosa is a group of heritable skin fragility disorders with considerable morbidity and mortality. It is known to be caused by mutations in as... 
BONE-MARROW-TRANSPLANTATION | MESENCHYMAL CELLS | VII COLLAGEN | OSTEOGENESIS IMPERFECTA | SKIN | CHILDREN | DERMATOLOGY | Epidermolysis Bullosa - therapy | Epidermolysis Bullosa - genetics | Stem Cell Transplantation - methods | Humans | Genetic Therapy - methods
Journal Article
Journal Article
Journal Article
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, ISSN 1610-0379, 11/2015, Volume 13, Issue 11, pp. 1125 - 1133
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 04/2012, Volume 366, Issue 16, pp. 1508 - 1514
Three patients with homozygous mutations in the integrin α3 gene, a transmembrane integrin receptor subunit, were found to have disrupted basement-membrane... 
Congenital diseases | Kidneys | Epidermolysis bullosa | Laboratories | Lung diseases | Genes | Nephrotic syndrome | Patients | Peritoneal dialysis | Radiography | Babies | Pathology | Parents & parenting | Microscopy | Biopsy | Rodents | Skin diseases | Skin | Mutation | Age
Journal Article