The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen

Peter C. van den Akker*, Jemima E. Mellerio, Anna E. Martinez, Lu Liu, Rowdy Meijer, Patricia J. C. Dopping-Hepenstal, Anthonie J. van Essen, Hans Scheffer, Robert M. W. Hofstra, John A. McGrath, Marcel F. Jonkman

*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

30 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology

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