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Lipoid Proteinosis: Identification of Two Novel Mutations in the Human ECM-1 Gene and Lack of Genotype-Phenotype Correlation

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Coincident Two Mutations and One Single Nucleotide Polymorphism of the PTCH1 Gene in a Family with Naevoid Basal Cell Carcinoma Syndrome

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A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ–Siemens–Touraine syndrome

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Absence of Functional Mutations in the Ferroportin-encoding SLC40A1 Gene in Porphyria Cutanea Tarda: A Series of 37 Cases from Southern France

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