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: Contribution to journal › Letter › peer-review

10 Scopus citations

Original language	English (US)
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

All Science Journal Classification (ASJC) codes

Dermatology

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10.1111/j.1365-2133.2012.11181.x

Cite this

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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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language = "English (US)",

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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

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DO - 10.1111/j.1365-2133.2012.11181.x

M3 - Letter

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AN - SCOPUS:84873172827

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ER -

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

All Science Journal Classification (ASJC) codes

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