TY  - GEN
AU  - Martignago,B C F
AU  - Lai-Cheong,J E
AU  - Liu,L
AU  - McGrath,J A
AU  - Cestari,T F
TI  - Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome
SN  - 0007-0963
PY  - 2008///0410
KW  - Female
KW  - Genetic Carrier Screening
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - genetics
KW  - Mutation
KW  - Neoplasm Proteins
KW  - Pedigree
KW  - Skin Diseases, Genetic
KW  - Syndrome
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1365-2133.2007.08219.x
ER  -