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The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in...

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313572459

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model

About this item

Full title

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model

Publisher

United States: Public Library of Science

Journal title

PLoS genetics, 2012-05, Vol.8 (5), p.e1002724-e1002724

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Down syndrome (DS) leads to complex phenotypes and is the main genetic cause of birth defects and heart diseases. The Ts65Dn DS mouse model is trisomic for the distal part of mouse chromosome 16 and displays similar features with post-natal lethality and cardiovascular defects. In order to better understand these defects, we defined electrocardiogr...

Alternative Titles

Full title

The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1313572459

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1313572459

Other Identifiers

ISSN

1553-7404,1553-7390

E-ISSN

1553-7404

DOI

10.1371/journal.pgen.1002724

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