dc.contributor.author | Kim-Howard, Xana | |
dc.contributor.author | Sun, Celi | |
dc.contributor.author | Molineros, Julio E. | |
dc.contributor.author | Maiti, Amit K. | |
dc.contributor.author | Chandru, Hema | |
dc.contributor.author | Adler, Adam | |
dc.contributor.author | Wiley, Graham B. | |
dc.contributor.author | Kaufman, Kenneth M. | |
dc.contributor.author | Kottyan, Leah | |
dc.contributor.author | Guthridge, Joel M. | |
dc.contributor.author | Rasmussen, Astrid | |
dc.contributor.author | Kelly, Jennifer | |
dc.contributor.author | Sánchez, Elena | |
dc.contributor.author | Raj, Prithvi | |
dc.contributor.author | Li, Quan-Zhen | |
dc.contributor.author | Bang, So-Young | |
dc.contributor.author | Lee, Hye-Soon | |
dc.contributor.author | Kim, Tae-Hwan | |
dc.contributor.author | Kang, Young Mo | |
dc.contributor.author | Suh, Chang-Hee | |
dc.contributor.author | Chung, Won Tae | |
dc.contributor.author | Park, Yong-Beom | |
dc.contributor.author | Choe, Jung-Yoon | |
dc.contributor.author | Shim, Seung Cheol | |
dc.contributor.author | Lee, Shin-Seok | |
dc.contributor.author | Han, Bok-Ghee | |
dc.contributor.author | Olsen, Nancy J. | |
dc.contributor.author | Karp, David R. | |
dc.contributor.author | Moser, Kathy | |
dc.contributor.author | Pons-Estel, Bernardo A. | |
dc.contributor.author | Wakeland, Edward K. | |
dc.contributor.author | James, Judith A. | |
dc.contributor.author | Harley, John B. | |
dc.contributor.author | Bae, Sang-Cheol | |
dc.contributor.author | Gaffney, Patrick M. | |
dc.contributor.author | Alarcón-Riquelme, Marta | |
dc.contributor.author | Looger, Loren L. | |
dc.contributor.author | Nath, Swapan K. | |
dc.contributor.author | Acevedo-Vasquez, Eduardo | |
dc.contributor.author | GENLES Network Group | |
dc.date.accessioned | 2019-04-26T15:28:58Z | |
dc.date.available | 2019-04-26T15:28:58Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Human Molecular Genetics | es_PE |
dc.identifier.uri | https://hdl.handle.net/20.500.12959/490 | |
dc.description.abstract | Se realizó un análisis exhaustivo, utilizando un mapeo fino denso, para identificar variantes robustas e independientes que predisponen el Lupus Eritematoso Sistémico (LES), para predecir y validar los efectos moleculares de los alelos de riesgo de LES a través de la bioinformática, modelización molecular, y ensayos in vitro. Se analizó una gran cohorte multiétnica para investigar a fondo la asociación lupus eritematoso sistémico-NCF2 en población étnica diversa y para identificar etnicidad específica y variantes causales robustas. | es_PE |
dc.format | application/pdf | es_PE |
dc.language.iso | eng | es_PE |
dc.publisher | Seguro Social de Salud (EsSalud) | es_PE |
dc.rights | info:eu-repo/semantics/openAccess | es_PE |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | es_PE |
dc.source | Seguro Social de Salud (EsSalud) | es_PE |
dc.source | Repositorio Institucional EsSalud | es_PE |
dc.subject | Reumatología | es_PE |
dc.subject | Lupus Eritematoso Sistémico | es_PE |
dc.subject | Genética Humana | es_PE |
dc.title | Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations | es_PE |
dc.type | info:eu-repo/semantics/article | es_PE |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.05.00 | es_PE |
dc.publisher.country | PE | es_PE |