Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a...

British Journal of Dermatology 2007 Vol. 157; Iss. 6

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

B.C.F. Martignago, J.E. Lai-Cheong, L. Liu, J.A. Mc Grath, T.F. Cestari
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
157
Year:
2007
Language:
english
Pages:
4
DOI:
10.1111/j.1365-2133.2007.08219.x
File:
PDF, 411 KB
english, 2007
Conversion to is in progress
Conversion to is failed