Publicaciones de interés
SELECCIÓN DE LAS MEJORES PUBLICACIONES EN LOS ÚLTIMOS 5 AÑOS:
2013
1. Gandía M et al. A novel splice-site mutation in the GJB2 gene causing mild postlingual hearing impairment. PloS ONE. 2013 Sep. doi: 10.1371/journal.pone.0073566. eCollection 2013.
PMID: 24039984
https://www.ncbi.nlm.nih.gov/pubmed/24039984
2014
2. P Kevin Legan et al. Three Deaf Mice: Mouse Models for TECTA-based Human Hereditary Deafness Reveal Domain-specific Structural Phenotypes in the Tectorial Membrane. Human Molecular Genetics. 2014 May. doi: 10.1093/hmg/ddt646.
PMID: 24363064
https://www.ncbi.nlm.nih.gov/pubmed/24363064
2015
3. M Gandía et al. Mutations in PRPS1 causing syndromic or nonsyndromic hearing impairment: intrafamilial phenotypic variation complicates genetic counseling. Pediatric Research. 2015 Jul. doi: 10.1038/pr.2015.56.
PMID: 25785835
https://www.ncbi.nlm.nih.gov/pubmed/25785835
4. Celia Zaro, et al. Allelic mutations of KITLG, encoding KIT ligand, cause asymmetric and unilateral hearing los and Waardenburg síndrome type II. American Journal of Human Genetics. 2015 Nov. doi: 10.1016/j.ajhg.2015.09.011.
PMID: 26522471
https://www.ncbi.nlm.nih.gov/pubmed/26522471
2017
5. Marin AV, et al. Primary T-cell immunodeficiency with functional revertant somatic mosaicism in CD247. J Allergy Clin Immunol. Jan 2017. doi: 10.1016/j.jaci.2016.06.020.
PMID: 27555457
https://www.ncbi.nlm.nih.gov/pubmed/27555457
2018
6. Wesdorp M, et al. MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse. Am J Um Genet. 2018 Jul. doi: 10.1016/j.ajhg.2018.05.011
PMID: 29961571