SLC5A5 mutation.xlsx
收藏官方服务：
资源简介：
Two hundred and seventy-three patients with primary congenital hypothyroidism were screened for mutations in <i>SLC5A5 </i>by next-generation sequencing. <br>
提供机构：
figshare创建时间：
2020-10-23
社区交流群
科研交流群
商业服务
Two hundred and seventy-three patients with primary congenital hypothyroidism were screened for mutations in <i>SLC5A5 </i>by next-generation sequencing. <br>