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5. A de novo variant in the ASPRV1 gene in a dog with ichthyosis. Bauer A; Waluk DP; Galichet A; Timm K; Jagannathan V; Sayar BS; Wiener DJ; Dietschi E; Müller EJ; Roosje P; Welle MM; Leeb T PLoS Genet; 2017 Mar; 13(3):e1006651. PubMed ID: 28249031 [TBL] [Abstract][Full Text] [Related]
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10. Compound heterozygous missense mutations p.Leu207Pro and p.Tyr544Cys in TGM1 cause a severe form of lamellar ichthyosis. Takeda M; Nomura T; Sugiyama T; Miyauchi T; Suzuki S; Fujita Y; Shimizu H J Dermatol; 2018 Dec; 45(12):1463-1467. PubMed ID: 30302839 [TBL] [Abstract][Full Text] [Related]
11. Aberrant lipid organization in stratum corneum of patients with atopic dermatitis and lamellar ichthyosis. Pilgram GS; Vissers DC; van der Meulen H; Pavel S; Lavrijsen SP; Bouwstra JA; Koerten HK J Invest Dermatol; 2001 Sep; 117(3):710-7. PubMed ID: 11564181 [TBL] [Abstract][Full Text] [Related]
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14. Autosomal-dominant lamellar ichthyosis: ultrastructural characteristics of a new type of congenital ichthyosis. Kolde G; Happle R; Traupe H Arch Dermatol Res; 1985; 278(1):1-5. PubMed ID: 4096524 [TBL] [Abstract][Full Text] [Related]
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17. Autosomal dominant lamellar ichthyosis: a new skin disorder. Traupe H; Kolde G; Happle R Clin Genet; 1984 Nov; 26(5):457-61. PubMed ID: 6499258 [TBL] [Abstract][Full Text] [Related]