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

Producción científica: Artículos / Notas › Carta › revisión exhaustiva

11 Citas (Scopus)

Idioma original	Inglés
Páginas (desde-hasta)	456-458
Número de páginas	3
Publicación	British Journal of Dermatology
Volumen	168
N.º	2
DOI	https://doi.org/10.1111/j.1365-2133.2012.11181.x
Estado	Publicada - feb. 2013

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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 - 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

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