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Nat Genet ; 43(12): 1186-8, 2011 Oct 23.
Article in English | MEDLINE | ID: mdl-22019780

ABSTRACT

Systemic lupus erythematosus (SLE) is a complex autoimmune disease that causes substantial morbidity. As is typical for many other multifactorial disorders, much of the heritability of SLE remains unknown. We identified a rare autosomal recessive form of SLE, in which autozygome analysis revealed a null mutation in the DNASE1L3 gene. The DNASE1L3-related SLE we describe was always pediatric in onset and correlated with a high frequency of lupus nephritis. Our findings confirm the critical role of impaired clearance of degraded DNA in SLE pathogenesis.


Subject(s)
Endodeoxyribonucleases/genetics , Lupus Erythematosus, Systemic/genetics , Sequence Deletion , Adolescent , Child , Child, Preschool , Consanguinity , Female , Genetic Association Studies , Heredity , Homozygote , Humans , Lod Score , Male , Young Adult
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