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Am J Hum Genet. 2007 Apr;80(4):811-5. Epub 2007 Feb 19.

Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.

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  • 1Leeds Institute of Molecular Medicine, St James's University Hospital, Leeds, LS9 7TF, UK.

Abstract

TREX1 constitutes the major 3'-->5' DNA exonuclease activity measured in mammalian cells. Recently, biallelic mutations in TREX1 have been shown to cause Aicardi-Goutieres syndrome at the AGS1 locus. Interestingly, Aicardi-Goutieres syndrome shows overlap with systemic lupus erythematosus at both clinical and pathological levels. Here, we report a heterozygous TREX1 mutation causing familial chilblain lupus. Additionally, we describe a de novo heterozygous mutation, affecting a critical catalytic residue in TREX1, that results in typical Aicardi-Goutieres syndrome.

PMID:
17357087
[PubMed - indexed for MEDLINE]
PMCID:
PMC1852703
Free PMC Article
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