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

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

13 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
Externally published	Yes

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10.1111/j.1365-2133.2012.11181.x

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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",

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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

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

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