Mostrar el registro sencillo del ítem

dc.contributor.authorBuffon, Marjoriê Piucopt_BR
dc.contributor.authorSortica, Denise Alvespt_BR
dc.contributor.authorGerchman, Fernandopt_BR
dc.contributor.authorCrispim, Daisypt_BR
dc.contributor.authorCanani, Luis Henrique Santospt_BR
dc.date.accessioned2019-07-10T02:34:44Zpt_BR
dc.date.issued2015pt_BR
dc.identifier.issn1758-5996pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/196750pt_BR
dc.description.abstractDiabetic kidney disease (DKD) is a chronic complication of diabetes mellitus, which is considered a worldwide epidemic. Several studies have been developed in order to elucidate possible genetic factors involved in this disease. The FRMD3 gene, a strong candidate selected from genome wide association studies (GWAS), encodes the structural protein 4.1O involved in maintaining cell shape and integrity. Some single nucleotide polymorphisms (SNPs) located in FRMD3 have been associated with DKD in different ethnicities. However, despite these findings, the matter is still controversial. The aim of this narrative review is to summarize the evidence regarding the role of FRMD3 in DKD.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofDiabetology and Metabolic Syndrome. São Paulo. Vol. 7, n. 118 (2015), 10 p.pt_BR
dc.rightsOpen Accessen
dc.subjectDiabetes mellituspt_BR
dc.subjectNefropatiaspt_BR
dc.subjectGenéticapt_BR
dc.titleFRMD3 gene : its role in diabetic kidney disease : a narrative reviewpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000984292pt_BR
dc.type.originEstrangeiropt_BR


Ficheros en el ítem

Thumbnail
   

Este ítem está licenciado en la Creative Commons License

Mostrar el registro sencillo del ítem