Targeted next-generation sequencing for congenital hypothyroidism with positive neonatal TSH screening_Supplemental_Data
收藏Figshare2020-02-22 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Targeted_next-generation_sequencing_for_congenital_hypothyroidism_with_positive_neonatal_TSH_screening_Supplemental_Data/11876388
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资源简介：
Genetic analysis of 24 causative genes using next-generation sequence in 167 Japanese patients. We identified 178 variants in 66.5% (111/167) cases in the fifteen genes, DUOX2, TSHR, PAX8, TG, TPO, DUOXA2, JAG1, GLIS3, DUOX1, IYD, SLC26A4, SLC5A5, SECISBP2, DIO1, and DIO3.
创建时间：
2020-02-22
