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Publications by C. Peret
Molecular Confirmation of the Unique Phenotype of Epidermolysis Bullosa Simplex With Mottled Pigmentation
British Journal of Dermatology
Dermatology
Medicine
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Epidermolysis Bullosa Simplex With Mottled Pigmentation: The First Slovenian Case
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Molecular Heterogeneity of Epidermolysis Bullosa Simplex: Contribution of EXPH5 Mutations
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Epidermolysis Bullosa Simplex, Generalized Intermediate
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The Genetic Basis of Weber-Cockayne Epidermolysis Bullosa Simplex.
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Epidermolysis Bullosa Simplex Due to BP230 Deficiency
Recessive Epidermolysis Bullosa Simplex- A Case Report
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