Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
- Resource Type
- Article
- Source
- Journal of Endocrinological Investigation; Apr2022, Vol. 45 Issue 4, p773-786, 14p
- Subject
- Language
- ISSN
- 03914097