Hernando Mosquera Sanchez

Research activity per year

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2015
A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis
Ortega-Recalde, O., Moreno, M. B., Vergara, J. I., Fonseca, D. J., Rojas, R. F., Mosquera, H., Medina, C. L., Restrepo, C. M. & Laissue, P., 1 Oct 2015, In: Clinical and Experimental Dermatology. 40, 7, p. 757-760 4 p.
Research output: Articles / Notes › Scientific Article › peer-review
4 Scopus citations
2013
Whole-Exome Sequencing Enables Rapid Determination of Xeroderma Pigmentosum Molecular Etiology
Ortega-Recalde, O., Vergara, J. I., Fonseca, D. J., Ríos, X., Mosquera, H., Bermúdez, O. M., Medina, C. L., Vargas, C. I., Pallares, A. E., Restrepo, C. M. & Laissue, P., 3 Jun 2013, In: PLoS ONE. 8, 6, e64692.
Research output: Articles / Notes › Scientific Article › peer-review

Open Access
20 Scopus citations

Research output