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Publications by H Steinke
Homozygous Nonsense Mutation and Additional Deletion of an Amino Acid in BPAG1e Causing Mild Localized Epidermolysis Bullosa Simplex
Acta Dermato-Venereologica
Dermatology
Medicine
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The Genetic Basis of Weber-Cockayne Epidermolysis Bullosa Simplex.
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Image Gallery: Multiple Localized Lipoatrophy in Recessive Dystrophic Epidermolysis Bullosa
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Molecular Heterogeneity of Epidermolysis Bullosa Simplex: Contribution of EXPH5 Mutations
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