Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus

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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. © 2011 Nature America, Inc. All rights reserved.

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Al-Mayouf, S. M., Sunker, A., Abdwani, R., Abrawi, S. A., Almurshedi, F., Alhashmi, N., … Alkuraya, F. S. (2011). Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus. Nature Genetics, 43(12), 1186–1188. https://doi.org/10.1038/ng.975

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