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The App-Runx1 Region Is Critical for Birth Defects and Electrocardiographic Dysfunctions Observed in a Down Syndrome Mouse Model
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 un...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2012
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3364940/ https://ncbi.nlm.nih.gov/pubmed/22693452 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1002724 |
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