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6. Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation. Abdollahimajd F; Rajabi F; Shahidi-Dadras M; Saket S; Youssefian L; Vahidnezhad H; Uitto J Br J Dermatol; 2019 Sep; 181(3):584-586. PubMed ID: 30307612 [TBL] [Abstract][Full Text] [Related]
7. The phenotypic and molecular genetic features of pachyonychia congenita. McLean WH; Hansen CD; Eliason MJ; Smith FJ J Invest Dermatol; 2011 May; 131(5):1015-7. PubMed ID: 21430705 [TBL] [Abstract][Full Text] [Related]
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12. Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders. Li P; Qi J; Zhong Y; Ding A; Xiao H J Proteomics; 2023 Sep; 287():104971. PubMed ID: 37467889 [TBL] [Abstract][Full Text] [Related]
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15. Two for two: Dual therapy with erlotinib and acitretin for twins with severe keratoderma in Olmsted syndrome. Butala S; Phan S; Siegel DH; Carlberg V; Paller AS Pediatr Dermatol; 2023; 40(4):735-737. PubMed ID: 36709954 [TBL] [Abstract][Full Text] [Related]
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