弥漫性皮肤系统性硬化症的家族性聚集 : C1r 基因缺陷的相互作用 ,易感 HLA 单倍型和自身抗体。
Mesh : Humans Genetic Predisposition to Disease Autoantibodies / blood Haplotypes Scleroderma, Diffuse / genetics immunology diagnosis blood Female Pedigree Phenotype Male Complement C1 Inhibitor Protein / genetics Risk Factors Adult Mutation Middle Aged HLA Antigens / genetics immunology
来 源: DOI:10.1111/1756-185X.15247