Compound Heterozygosity for Silent and Dominant Glycine Substitution Mutations in COL7A1 Leads to a Marked Transient Intracytoplasmic Retention of Procollagen VII and a Moderately Severe Dystrophic Epidermolysis Bullosa Phenotype

Abstract
No abstract available
Funding Information
  • Deutsche Forschungsgemeinschaft
  • Ministry of Education, Culture, Sports, Science and Technology (1475/2–3)
  • Dystrophic Epidermolysis Bullosa Research Association

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