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4. Case of Kindler syndrome resulting from mutation in the FERMT1 gene. Wada M; Masuda K; Tsuruta D; Tamai K; Lai-Cheong JE; McGrath JA; Katoh N J Dermatol; 2012 Dec; 39(12):1057-8. PubMed ID: 22672060 [No Abstract] [Full Text] [Related]
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10. Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome. Natsuga K; Nishie W; Shinkuma S; Nakamura H; Matsushima Y; Tatsuta A; Komine M; Shimizu H J Dermatol Sci; 2011 Jan; 61(1):38-44. PubMed ID: 21146372 [TBL] [Abstract][Full Text] [Related]
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20. Novel and recurrent FERMT1 gene mutations in Kindler syndrome. Techanukul T; Sethuraman G; Zlotogorski A; Horev L; Macarov M; Trainer A; Fong K; Lens M; Medenica L; Ramesh V; McGrath JA; Lai-Cheong JE Acta Derm Venereol; 2011 May; 91(3):267-70. PubMed ID: 21336475 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]