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Spontaneous partial loss of the OT-I transgene Next article Nature Immunology | News and Views A dendritic cell subset designed for oral tolerance A human inborn error connects the α's Isabelle Meyts1, Jean-Laurent Casanova2, Affiliations Corresponding author Journal name: Nature Immunology Volume: 17, Pages: 472–474 Year published: (2016) DOI: doi:10.1038/ni.3420 Published online 19 April
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2016 Article tools Citation Reprints Rights & permissions Article metrics Patients with XLPDR are found to carry an intronic hypomorphic mutation in the gene encoding the catalytic subunit of DNA polymerase-α. Patients' cells display low levels of cytoplasmic RNA:DNA hybrids, which increases the expression of interferon-α-induced genes, a hallmark of monogenic 'type I interferonopathies'. Subject terms: Innate immunity• Primary immunodeficiency disorders• Translational immunology Read the full article Subscribe to Nature Immunology for full access: $225 Subscribe Purchase article full text and PDF: $18 Buy now Already a subscriber? Log in now or Register for online access. Additional access options: Use a document delivery service Login via OpenAthens Purchase a site license Institutional access British Library Document Supply Centre You can also request this document from your local library through inter-library loan services. References References• Author information Partington, M.W., Marriott, P.J., Prentice, R.S., Cavaglia, A. & Simpson, N.E. Am. J. Med. Genet. 10, 65–75 (1981). CAS PubMed Article Starokadomskyy, A
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