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. Novel and recurrent FERMT1 gene mutations in Kindler syndrome. Acta Derm Venereol. 2011 May; 91(3):267-70.

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