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少汗性外胚层发育不良患者EDA基因突变检测及表型分析
OBJECTIVE: To detect the ectodysplasin A (EDA) gene mutation in patients with hypohidro-tic ectodermal dysplasia (HED), and to analyze the distribution pattern of missing permanent teeth and the systemic manifestation of HED patients with EDA gene mutation. METHODS: Twelve HED families were enrolled...
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| Publicado en: | Beijing Da Xue Xue Bao Yi Xue Ban |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
北京大学学报(医学版)编辑部
2021
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7867966/ https://ncbi.nlm.nih.gov/pubmed/33550332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.19723/j.issn.1671-167X.2021.01.005 |
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