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3279 First in Man

3279 First in Man

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_37f04d83e8a44add93c8d4df0bce6e5b

3279 First in Man

About this item

Full title

3279 First in Man

Publisher

Cambridge: Cambridge University Press

Journal title

Journal of clinical and translational science, 2019-03, Vol.3 (s1), p.45-45

Language

English

Formats

Publication information

Publisher

Cambridge: Cambridge University Press

More information

Scope and Contents

Contents

OBJECTIVES/SPECIFIC AIMS: A mimic of congenital infections and a rare genetic cause of interferon overproduction, Aicardi Goutières Syndrome (AGS) results in significant neurologic disability. AGS is caused by pathogenic changes in the intracellular nucleic acid sensing machinery (TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1, and IFIH1). All...

Alternative Titles

Full title

3279 First in Man

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_37f04d83e8a44add93c8d4df0bce6e5b

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_37f04d83e8a44add93c8d4df0bce6e5b

Other Identifiers

ISSN

2059-8661

E-ISSN

2059-8661

DOI

10.1017/cts.2019.107

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