| Idioma original | Inglés estadounidense |
|---|---|
| Páginas (desde-hasta) | 1372-1375 |
| Número de páginas | 4 |
| Publicación | British Journal of Dermatology |
| DOI | |
| Estado | Publicada - dic 1 2016 |
Citar esto
Ortega-Recalde, O., Silgado, D., Fetiva, C., Fonseca, D. J., & Laissue, P. (2016). Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation. British Journal of Dermatology, 1372-1375. https://doi.org/10.1111/bjd.14969
@article{58f5f91e2a1746a09a29c005f8148e91,
title = "Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation",
author = "O. Ortega-Recalde and D. Silgado and C. Fetiva and Fonseca, {D. J.} and P. Laissue",
year = "2016",
month = "12",
day = "1",
doi = "10.1111/bjd.14969",
language = "English (US)",
pages = "1372--1375",
journal = "British Journal of Dermatology",
issn = "0007-0963",
publisher = "Wiley-Blackwell",
}
Ortega-Recalde, O, Silgado, D, Fetiva, C, Fonseca, DJ & Laissue, P 2016, 'Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation', British Journal of Dermatology, pp. 1372-1375. https://doi.org/10.1111/bjd.14969
Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation. / Ortega-Recalde, O.; Silgado, D.; Fetiva, C.; Fonseca, D. J.; Laissue, P.
En: British Journal of Dermatology, 01.12.2016, p. 1372-1375.Resultado de la investigación: Contribución a una revista › Carta
TY - JOUR
T1 - Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation
AU - Ortega-Recalde, O.
AU - Silgado, D.
AU - Fetiva, C.
AU - Fonseca, D. J.
AU - Laissue, P.
PY - 2016/12/1
Y1 - 2016/12/1
U2 - 10.1111/bjd.14969
DO - 10.1111/bjd.14969
M3 - Letter
C2 - 27518765
SP - 1372
EP - 1375
JO - British Journal of Dermatology
JF - British Journal of Dermatology
SN - 0007-0963
ER -
Ortega-Recalde O, Silgado D, Fetiva C, Fonseca DJ, Laissue P. Transcriptomic analysis of skin in a case of ichthyosis Curth–Macklin caused by a KRT1 mutation. British Journal of Dermatology. 2016 dic 1;1372-1375. https://doi.org/10.1111/bjd.14969