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52. Erythropoietic protoporphyria: a new mutation responsible for exon skipping in the human ferrochelatase gene. Remenyik E; Lanyon GW; Horkay I; Paragh G; Wikonkál N; Kósa A; Moore MR J Invest Dermatol; 1998 Sep; 111(3):540-1. PubMed ID: 9740256 [No Abstract] [Full Text] [Related]
53. Human erythropoietic protoporphyria: identification of a mutation at the splice donor site of intron 7 causing exon 7 skipping of the ferrochelatase gene. Nakahashi Y; Miyazaki H; Kadota Y; Naitoh Y; Inoue K; Yamamoto M; Hayashi N; Taketani S Hum Mol Genet; 1993 Jul; 2(7):1069-70. PubMed ID: 8364548 [No Abstract] [Full Text] [Related]