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Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism.
JCI Insight. 2018 Oct 18;3(20):e99631. doi: 10.1172/jci.insight.99631.
JCI Insight. 2018.
PMID: 30333321
Free PMC article.
The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice.
Yamaguchi N, Suzuki A, Yoshida A, Tanaka T, Aoyama K, Oishi H, Hara Y, Ogi T, Amano I, Kameo S, Koibuchi N, Shibata Y, Ugawa S, Mizuno H, Saitoh S.
Yamaguchi N, et al.
Sci Rep. 2022 Jul 4;12(1):11259. doi: 10.1038/s41598-022-15151-4.
Sci Rep. 2022.
PMID: 35788623
Free PMC article.
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