Novel SLC16A2 mutations impair thyroid hormone transport and drive neurodevelopmental deficits in Chinese patients with allan-herndon-dudley syndrome
Summary
The online version contains supplementary material available at 10.1038/s41598-026-40703-3.
| Authors | Sun X, Wang C, Lin L, Lan X, Wu S, Chen X, Cai C |
|---|---|
| Journal | Scientific reports |
| Publication Date | 2026 Mar 1;16(1) |
| PubMed | 41765929 |
| PubMed Central | PMC13056955 |
| DOI | 10.1038/s41598-026-40703-3 |