whole-exome sequencing (WES) of patients with non-syndromic oligodontia
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资源简介：
To investigate pathogenic mutations of the paired box 9 (PAX9) gene in patients with non-syndromic oligodontia, and the functional impact of these mutations. WES was utilised to detect gene mutations in a cohort of patients diagnosed with non-syndromic oligodontia
创建时间：
2020-06-08
