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

Resultado de la investigación: Contribución a RevistaCarta

9 Citas (Scopus)
Idioma originalEnglish (US)
Páginas (desde-hasta)456-458
Número de páginas3
PublicaciónBritish Journal of Dermatology
DOI
EstadoPublished - feb 1 2013

Citar esto

Fonseca, D. J. ; Rojas, R. F. ; Vergara, J. I. ; Ríos, X. ; Uribe, C. ; Chávez, L. ; Velandia, F. ; Vargas, C. I. ; Restrepo, C. M. ; Laissue, Paul. / A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene. En: British Journal of Dermatology. 2013 ; pp. 456-458.
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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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A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene. / Fonseca, D. J.; Rojas, R. F.; Vergara, J. I.; Ríos, X.; Uribe, C.; Chávez, L.; Velandia, F.; Vargas, C. I.; Restrepo, C. M.; Laissue, Paul.

En: British Journal of Dermatology, 01.02.2013, p. 456-458.

Resultado de la investigación: Contribución a RevistaCarta

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 - 2013/2/1

Y1 - 2013/2/1

U2 - 10.1111/j.1365-2133.2012.11181.x

DO - 10.1111/j.1365-2133.2012.11181.x

M3 - Letter

C2 - 22834809

SP - 456

EP - 458

JO - British Journal of Dermatology

JF - British Journal of Dermatology

SN - 0007-0963

ER -