Associated Papers
A novel large FERMT1 (KIND1) gene deletion in Kindler syndrome.
Has C et al.
Journal of Dermatological Science, 2008
Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.
Martignago BC et al.
The British Journal of Dermatology, 2007
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