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2. Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia. Yamamoto M; Tsuda T; Otaki Y; Nakanishi T; Yamanishi K J Dermatol; 2012 Aug; 39(8):716-8. PubMed ID: 22035476 [No Abstract] [Full Text] [Related]
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4. An appraisal of acitretin therapy in children with inherited disorders of keratinization. Lacour M; Mehta-Nikhar B; Atherton DJ; Harper JI Br J Dermatol; 1996 Jun; 134(6):1023-9. PubMed ID: 8763418 [TBL] [Abstract][Full Text] [Related]
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11. Generalized and naevoid epidermolytic ichthyosis in Denmark: clinical and mutational findings. Bygum A; Virtanen M; Brandrup F; Gånemo A; Sommerlund M; Strauss G; Vahlquist A Acta Derm Venereol; 2013 May; 93(3):309-13. PubMed ID: 22930352 [TBL] [Abstract][Full Text] [Related]
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20. A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma. Suga Y; Duncan KO; Heald PW; Roop DR J Invest Dermatol; 1998 Dec; 111(6):1220-3. PubMed ID: 9856845 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]