期刊
JOURNAL OF INVESTIGATIVE DERMATOLOGY
卷 130, 期 7, 页码 1778-1784出版社
ELSEVIER SCIENCE INC
DOI: 10.1038/jid.2010.90
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- DEBRA Austria in coordination with DEBRA International
Epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of blistering disorders with considerable morbidity and mortality. Two decades ago, EB entered the molecular era with the identification of mutations in specific genes expressed within the cutaneous basement membrane zone; mutations in 14 genes have now been identified. This progress has now formed the basis for development of novel molecular therapies for this disease.
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