Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome
- 1 December 2007
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 157 (6) , 1281-1284
- https://doi.org/10.1111/j.1365-2133.2007.08219.x
Abstract
No abstract availableKeywords
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