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
    • Jouni Uitto

研究成果: Article › 同行評審

55   !!Link opens in a new tab 引文 斯高帕斯（Scopus）

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Biochemistry, Genetics and Molecular Biology