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. Case of Kindler syndrome resulting from mutation in the FERMT1 gene. J Dermatol. 2012 Dec; 39(12):1057-8.

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John McGrath

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