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The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen
  1. Correspondence to Dr Peter C van den Akker, Department of Genetics, University Medical Center Groningen, Hanzeplein 1, PO Box 30.001, 9700 RB Groningen, The Netherlands; p.c.van.den.akker{at}medgen.umcg.nl
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van den Akker PC, Mellerio JE, Martinez AE, et al
The inversa type of recessive dystrophic epidermolysis bullosa is caused by specific arginine and glycine substitutions in type VII collagen

Publication history

  • Received June 21, 2010
  • Revised September 1, 2010
  • Accepted September 23, 2010
  • First published November 26, 2010.
Online issue publication 
February 15, 2011

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