Literature DB >> 29722267

Recommendations to report and interpret HLA genetic findings in coeliac disease.

Concepción Núñez1, José Antonio Garrote2, Eduardo Arranz3, José Ramón Bilbao4, Fernando Fernández Bañares5, Juana Jiménez6, Teresa Perucho7, Eva Ruiz Casares7, Félix Sánchez-Valverde8, Juan I Serrano9.   

Abstract

Coeliac disease (CD) is a chronic autoimmune enteropathy triggered by gluten and related prolamines in genetically predisposed individuals. Although CD is a polygenic disease, there is a strong association with genes of the human leukocyte antigen (HLA) region. Most patients present the HLA-DQ2 heterodimer, specifically the DQ2.5 isoform, which is present in around 90-96% of patients of European ancestry.

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Year:  2018        PMID: 29722267     DOI: 10.17235/reed.2018.5269/2017

Source DB:  PubMed          Journal:  Rev Esp Enferm Dig        ISSN: 1130-0108            Impact factor:   2.086


  1 in total

Review 1.  Next-Generation Sequencing Based HLA Typing: Deciphering Immunogenetic Aspects of Sarcoidosis.

Authors:  Amit Kishore; Martin Petrek
Journal:  Front Genet       Date:  2018-10-25       Impact factor: 4.599

  1 in total

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