Article

Influence of COL9A1 and COL19A1 Polymorphisms on Kaschin-Beck Disease Risk

2020-02-06

Abstract excerpt

<title>Abstract</title> <p>Objective We aimed to determine whether COL9A1 and COL19A1 polymorphisms were associated with Kaschin-Beck disease (KBD) risk. Methods Five single nucleotide polymorphisms (SNPs) in COL9A1 and COL19A1 were genotyped in 316 KBD patients and 320 healthy controls using the Agena MassARRAY platform. The association between genetic polymorphisms ( COL9A1 : rs3806093, rs603410 and rs621347; C...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: d0b104f5-127a-5555-814f-658a52a260fd
DOI: 10.21203/rs.2.17278/v2

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Influence of COL9A1 and COL19A1 Polymorphisms on Kaschin-Beck Disease RiskDOI 10.21203/rs.2.17278/v2Read

Influence of COL9A1 and COL19A1 Polymorphisms on Kaschin-Beck Disease RiskSemantic proximity Read

COL9A1 gene polymorphism is associated with Kashin-Beck disease in a northwest Chinese Han population.Semantic proximity Read

Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease.Semantic proximity Read

Field synopsis and meta-analyses of genetic epidemiological evidence for Kashin-Beck disease, an endemic osteoarthropathy in China.Semantic proximity Read

A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease.Semantic proximity Read

Evaluation of the relationship and genetic overlap between Kashin-Beck disease and body mass index.Semantic proximity Read

Investigation of MMP-1 genetic polymorphisms and protein expression and their effects on the risk of Kashin-Beck disease in the northwest Chinese Han population.Semantic proximity Read

Genome-wide association study identifies COL2A1 locus involved in the hand development failure of Kashin-Beck disease.Semantic proximity Read

Exome sequencing identified FGF12 as a novel candidate gene for Kashin-Beck disease.Semantic proximity Read

Genome-wide copy number variation study and gene expression analysis identify ABI3BP as a susceptibility gene for Kashin-Beck disease.Semantic proximity Read

Genome-wide association study identifies ITPR2 as a susceptibility gene for Kashin-Beck disease in Han Chinese.Semantic proximity Read

[Association between polymorphism in DVWA and IL-1beta and Kashin-Beck disease].Semantic proximity Read