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 McGrath, T F Cestari

Research output: Contribution to journal › Letter › peer-review

16 Citations (Scopus)

Original language	English
Pages (from-to)	1281 - 1284
Number of pages	4
Journal	British Journal of Dermatology
Volume	157
Issue number	6
DOIs	https://doi.org/10.1111/j.1365-2133.2007.08219.x
Publication status	Published - Dec 2007

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

author = "Martignago, {B C F} and Lai-Cheong, {J E} and L Liu and McGrath, {J A} and Cestari, {T F}",

year = "2007",

month = dec,

doi = "10.1111/j.1365-2133.2007.08219.x",

language = "English",

volume = "157",

pages = "1281 -- 1284",

journal = "British Journal of Dermatology",

issn = "1365-2133",

publisher = "John Wiley & Sons, Ltd (10.1111)",

number = "6",

}

TY - JOUR

T1 - Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome

AU - Martignago, B C F

AU - Lai-Cheong, J E

AU - Liu, L

AU - McGrath, J A

AU - Cestari, T F

PY - 2007/12

Y1 - 2007/12

U2 - 10.1111/j.1365-2133.2007.08219.x

DO - 10.1111/j.1365-2133.2007.08219.x

M3 - Letter

SN - 1365-2133

VL - 157

SP - 1281

EP - 1284

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 6

ER -