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Identification of RUNX2 variants associated with cleidocranial dysplasia
BACKGROUND: Cleidocranial dysplasia (CCD) is a rare autosomal dominant disorder mainly characterized by hypoplastic or absent clavicles, delayed closure of the fontanelles, multiple dental abnormalities, and short stature. Runt-related transcription factor 2 (RUNX2) gene variants can cause CCD, but...
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| 出版年: | Hereditas |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6747736/ https://ncbi.nlm.nih.gov/pubmed/31548836 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s41065-019-0107-7 |
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