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
- Hassan Vahidnezhad
- , Leila Youssefian
- , Amir Hossein Saeidian
- , Andrew Touati
- , Sara Pajouhanfar
- , Taghi Baghdadi
- , Azam Ahmadi Shadmehri
- , Cecilia Giunta
- , Marius Kraenzlin
- , Delfien Syx
- , Fransiska Malfait
- , Cristina Has
- , Su M. Lwin
- , Razieh Karamzadeh
- , Lu Liu
- , Alyson Guy
- , Mohammad Hamid
- , Ariana Kariminejad
- , Sirous Zeinali
- , John A. McGrath
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斯高帕斯（Scopus）