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Article

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

11 Sept 2014

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Share to Cerebrovascular and genetic disorders
Share to Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Share to Ocular Diseases and Behçet’s Syndrome

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25213617
DOI: 10.1007/s10072-014-1944-9

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