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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
Formato: Artigo
Lenguaje:Inglês
Publicado: 北京大学学报(医学版)编辑部 2021
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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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