TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophy

The TREX1 C-terminal Region Controls Cellular Localization through Ubiquitination

(2013) Clinton D. Orebaugh et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Heterozygous TREX1 mutations in early-onset cerebrovascular disease

(2013) N. Pelzer et al.   JOURNAL OF NEUROLOGY

The Genetics of Small-Vessel Disease

(2012) A. Bersano et al.   CURRENT MEDICINAL CHEMISTRY

Hereditary cerebral small vessel diseases: A review

(2012) Antonio Federico et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

EVOLUTION OF A TUMOR-LIKE LESION IN CEREBRORETINAL VASCULOPATHY AND TREX1 MUTATION

(2010) F. J. Mateen et al.   NEUROLOGY

Biochemical properties of mammalian TREX1 and its association with DNA replication and inherited inflammatory disease: Figure 1

(2009) Tomas Lindahl et al.   BIOCHEMICAL SOCIETY TRANSACTIONS

Hereditary Systemic Angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathy

(2008) D. T. Winkler et al.   JOURNAL OF NEUROLOGY