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2. A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases. Chmel N; Danescu S; Gruler A; Kiritsi D; Bruckner-Tuderman L; Kreuter A; Kohlhase J; Has C J Invest Dermatol; 2015 Nov; 135(11):2876-2879. PubMed ID: 26083552 [No Abstract] [Full Text] [Related]
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19. A case of Kindler syndrome in a young Indian female with exon deletion. Fukushi R; Tsuboi R; Maeda T; Kanda Y; Sakai N; Suzuki S; Harada K Int J Dermatol; 2019 Jan; 58(1):e19-e21. PubMed ID: 30414177 [No Abstract] [Full Text] [Related]
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