Associated Papers
CTLA4 variants and haplotype contribute genetic susceptibility to myasthenia gravis in northern Chinese population.
Sun L et al.
Plos One, 2014
CTLA-4 exon 1 +49A/G polymorphism is associated with renal involvement in pediatric Henoch-Schönlein purpura.
Wang JJ et al.
Pediatric Nephrology (berlin, Germany), 2012
CTLA-4 exon 1 +49 polymorphism alone and in a haplotype with -318 promoter polymorphism may confer susceptibility to chronic HBV infection in Chinese Han patients.
Duan S et al.
Molecular Biology Reports, 2011
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