A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene

D. J. Fonseca; R. F. Rojas; J. I. Vergara; X. Ríos; C. Uribe; L. Chávez; F. Velandia; C. I. Vargas; C. M. Restrepo; Paul Laissue

doi:10.1111/j.1365-2133.2012.11181.x

A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene

D. J. Fonseca, R. F. Rojas, J. I. Vergara, X. Ríos, C. Uribe, L. Chávez, F. Velandia, C. I. Vargas, C. M. Restrepo, Paul Laissue

Especialización en Dermatología

Research output: Articles / Notes › Letter › peer-review

10 Scopus citations

Original language	English
Pages (from-to)	456-458
Number of pages	3
Journal	British Journal of Dermatology
Volume	168
Issue number	2
DOIs	https://doi.org/10.1111/j.1365-2133.2012.11181.x
State	Published - Feb 2013

Access to Document

10.1111/j.1365-2133.2012.11181.x

Cite this

@article{f551bfae291f49a1b68ac3ad7f8f7a01,

title = "A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene",

author = "Fonseca, {D. J.} and Rojas, {R. F.} and Vergara, {J. I.} and X. R{\'i}os and C. Uribe and L. Ch{\'a}vez and F. Velandia and Vargas, {C. I.} and Restrepo, {C. M.} and Paul Laissue",

year = "2013",

month = feb,

doi = "10.1111/j.1365-2133.2012.11181.x",

language = "Ingl{\'e}s",

volume = "168",

pages = "456--458",

journal = "British Journal of Dermatology",

issn = "0007-0963",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "2",

}

TY - JOUR

T1 - A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene

AU - Fonseca, D. J.

AU - Rojas, R. F.

AU - Vergara, J. I.

AU - Ríos, X.

AU - Uribe, C.

AU - Chávez, L.

AU - Velandia, F.

AU - Vargas, C. I.

AU - Restrepo, C. M.

AU - Laissue, Paul

PY - 2013/2

Y1 - 2013/2

UR - http://www.scopus.com/inward/record.url?scp=84873172827&partnerID=8YFLogxK

U2 - 10.1111/j.1365-2133.2012.11181.x

DO - 10.1111/j.1365-2133.2012.11181.x

M3 - Carta

C2 - 22834809

AN - SCOPUS:84873172827

SN - 0007-0963

VL - 168

SP - 456

EP - 458

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 2

ER -

A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene

Access to Document

Other files and links

Cite this