Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women. - Wikidata - wikimedia - TriplyDB

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

http://www.wikidata.org/entity/Q45398733

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Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases Systemic lupus erythematosus diagnostics in the 'omics' era Clinical implications of copy number variations in autoimmune disorders De novo copy number variations in cloned dogs from the same nuclear donor Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus.Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.Recapitulation of Candidate Systemic Lupus Erythematosus-Associated Variants in Koreans.Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations.Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.The complement system in systemic lupus erythematosus: an update.Types of DNA methylation status of the interspersed repetitive sequences for LINE-1, Alu, HERV-E and HERV-K in the neutrophils from systemic lupus erythematosus patients and healthy controls.Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis.Low copy number of FCGR3B is associated with lupus nephritis in a Chinese population.Genome-wide copy number variation analysis identifies deletion variants associated with ankylosing spondylitis.DNA methylation 101: what is important to know about DNA methylation and its role in SLE risk and disease heterogeneity

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P2860

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

http://www.wikidata.org/entity/Q45398733

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Deletion variants of RABGAP1L, ...... erythematosus in Korean women.

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Hae-Jin Hu

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Hye-Soon Lee

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Hyoung Doo Shin

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Ji-Hong Kim

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Joon Seol Bae

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Seon-Hee Yim

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Seung-Huyn Jung

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So-Yeon Park

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So-Young Bang

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Yeun-Jun Chung

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P2860

Structural variation in the human genome

Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs

Global variation in copy number in the human genome

Sensitive and specific real-time polymerase chain reaction assays to accurately determine copy number variations (CNVs) of human complement C4A, C4B, C4-long, C4-short, and RCCX modules: elucidation of C4 CNVs in 50 consanguineous subjects with defi

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

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The 1982 revised criteria for the classification of systemic lupus erythematosus

Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Copy number variants in genetic susceptibility and severity of systemic lupus erythematosus

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1055-1063

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10.1002/ART.37854

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