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Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5396125

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

About this item

Full title

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2017-04, Vol.7 (1), p.46454, Article 46454

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Pediatric inflammatory bowel disease (pIBD) is a chronic heterogeneous disorder. This study looks at the burden of common and rare coding mutations within 41 genes comprising the NOD signaling pathway in pIBD patients. 136 pIBD and 106 control samples underwent whole-exome sequencing. We compared the burden of common, rare and private mutation betw...

Alternative Titles

Full title

Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5396125

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5396125

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/srep46454

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