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Myasthenia gravis is an autoimmune immune disease, clinical manifestations of muscle weakness and fatigability
immunity
Early-onset (EO) and late-onset (LO) myasthenia gravis have obvious epidemiological and pathological features
The recent genome-wide association study ( GWAS ) found some genetic risk sites for myasthenia gravis, providing a glimpse into the underlying disease mechanism
GWAS
Recently, Lahiru Handunnetthi and others of the University of Oxford developed Priority Index, a genomics method that combines cell-type-specific functional genomic information, such as gene expression and chromatin organization, with the findings of GWAS to determine disease-related Gene
Developed Priority Index, a genomics method that combines cell type-specific functional genomic information, such as gene expression and chromatin organization, with the findings of GWAS to identify disease-related genes
It was also found that the regulator of toll-like receptor 4 signaling was only enriched in early-onset disease genes (fold enrichment = 3.
Two causal genetic variants were found near the CTLA4 gene (rs231770 and rs231735; posterior probability = 0.
The practical significance of this research is that the disease-related genes discovered in this research are unique resources in many disciplines, including clinicians, scientists, and the pharmaceutical industry
The disease-related genes discovered in this study are unique resources in many disciplines, including clinicians, scientists, and the pharmaceutical industry .
The disease-related genes discovered in this study are unique resources in many disciplines, including clinicians, scientists, and the pharmaceutical industry.
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