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11. Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome. Sprecher E; Tesfaye-Kedjela A; Ratajczak P; Bergman R; Richard G Clin Exp Dermatol; 2004 Sep; 29(5):513-7. PubMed ID: 15347338 [TBL] [Abstract][Full Text] [Related]