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33. Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation. Betlloch I; Lucas Costa A; Mataix J; Pérez-Crespo M; Ballester I Pediatr Dermatol; 2009; 26(4):489-91. PubMed ID: 19689541 [TBL] [Abstract][Full Text] [Related]
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35. [Systemic lupus erythematosus and antiphospholipid antibody syndrome in a patient with congenital ichthyosiform erythroderma]. Nishiyama S; Miyawaki S Ryumachi; 1995 Aug; 35(4):688-92. PubMed ID: 7482067 [TBL] [Abstract][Full Text] [Related]
36. A novel mutation in the 12(R)-lipoxygenase (ALOX12B) gene underlies nonbullous congenital ichthyosiform erythroderma. Ashoor G; Massé M; García Luciano LM; Sheffer R; Martinez-Mir A; Christiano AM; Zlotogorski A Br J Dermatol; 2006 Jul; 155(1):198-200. PubMed ID: 16792775 [No Abstract] [Full Text] [Related]
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