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β-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1
DiGeorge syndrome (DGS) is a common genetic disease characterized by pharyngeal apparatus malformations and defects in cardiovascular, craniofacial and glandular development. TBX1 is the most likely candidate disease-causing gene and is located within a 22q11.2 chromosomal deletion that is associate...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Company of Biologists
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2835329/ https://ncbi.nlm.nih.gov/pubmed/20215350 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.045534 |
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