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RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia
Cleidocranial dysplasia (CCD) is an autosomal dominant human skeletal disorder comprising hypoplastic clavicles, wide cranial sutures, supernumerary teeth, short stature, and other skeletal abnormalities. It is known that mutations in the human RUNX2 gene mapped at 6p21 are responsible for CCD. We a...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Sociedade Brasileira de Genética
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3115309/ https://ncbi.nlm.nih.gov/pubmed/21734816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1415-47572011005000002 |
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