Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome [10]

B. C.F. Martignago; J. E. Lai-Cheong; L. Liu; J. A. McGrath; T. F. Cestari

doi:10.1111/j.1365-2133.2007.08219.x

Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome [10]

B. C.F. Martignago, J. E. Lai-Cheong, L. Liu, J. A. McGrath, T. F. Cestari

Department of Dermatology

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 - 2007 Dec

All Science Journal Classification (ASJC) codes

Dermatology

Access to Document

10.1111/j.1365-2133.2007.08219.x

Cite this

@article{f6167b7b5cb1427db593a4829fad4d24,

title = "Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome [10]",

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 = "0007-0963",

publisher = "Wiley-Blackwell",

number = "6",

}

TY - JOUR

T1 - Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome [10]

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

UR - http://www.scopus.com/inward/record.url?scp=36148998088&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=36148998088&partnerID=8YFLogxK

U2 - 10.1111/j.1365-2133.2007.08219.x

DO - 10.1111/j.1365-2133.2007.08219.x

M3 - Letter

C2 - 17916195

AN - SCOPUS:36148998088

SN - 0007-0963

VL - 157

SP - 1281

EP - 1284

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 6

ER -

Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome [10]

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Cite this