Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome.

Martignago, B C F

Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome. [electronic resource] - The British journal of dermatology Dec 2007 - 1281-4 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

0007-0963

10.1111/j.1365-2133.2007.08219.x doi


Female
Genetic Carrier Screening
Humans
Male
Membrane Proteins--genetics
Mutation--genetics
Neoplasm Proteins--genetics
Pedigree
Skin Diseases, Genetic--genetics
Syndrome