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HIRA Gene is Lower Expressed in the Myocardium of Patients with Tetralogy of Fallot
BACKGROUND: The most typical cardiac abnormality is conotruncal defects (CTDs) in patients with 22q11 deletion syndrome (22q11DS). HIRA (histone cell cycle regulator) gene, as one of the candidate genes located at the critical region of 22q11DS, was reported as possibly relevant to CTD in animal mod...
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| Publicat a: | Chin Med J (Engl) |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Medknow Publications & Media Pvt Ltd
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5072250/ https://ncbi.nlm.nih.gov/pubmed/27748330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.191745 |
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