1995
DOI: 10.1136/ard.54.6.530
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Homozygous complement factor deficiency and primary antiphospholipid syndrome: a clinical and serological study.

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“…This association of primary APS with C4 null alleles was confirmed by other groups as well [16]. Homozygous C2 deficiency was identified in another individual with primary APS, whose sister had previously died at age 30 from myocardial infarction after years of migraine [17]. The genes for C2 and C4 are located within the major histocompatibility complex (MHC) on chromosome 6, and deficiency alleles are linked with an "autoimmune" extended MHC haplotype (HLA-B8, DR3) that itself has been linked to primary APS in other studies [18].…”
Section: Observations In People With Antiphospholipid Syndromesupporting
confidence: 66%
“…This association of primary APS with C4 null alleles was confirmed by other groups as well [16]. Homozygous C2 deficiency was identified in another individual with primary APS, whose sister had previously died at age 30 from myocardial infarction after years of migraine [17]. The genes for C2 and C4 are located within the major histocompatibility complex (MHC) on chromosome 6, and deficiency alleles are linked with an "autoimmune" extended MHC haplotype (HLA-B8, DR3) that itself has been linked to primary APS in other studies [18].…”
Section: Observations In People With Antiphospholipid Syndromesupporting
confidence: 66%