HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region
<p><strong>Rationale:</strong> 22q11 deletion syndrome arises from recombination between low-copy repeats on chromosome 22. Typical deletions result in hemizygosity for TBX1 associated with congenital cardiovascular disease. Deletions distal to the typically deleted region result i...
| Main Authors: | , , , , , , , |
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| Formato: | Journal article |
| Idioma: | English |
| Publicado em: |
American Heart Association
2014
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