Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency
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| Description | scientific article published on 18 November 2018 |
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author: Cecilia Giunta Alyson Guy Cristina Has Hassan Vahidnezhad Amir Hossein Saeidian S Zeinali John Mcgrath Ariana Kariminejad |
| Publication date | November 18, 2018 |
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