1. Stoupa A, Kariyawasam D, Polak M, Carré A. Genetics of congenital hypothyroidism: Modern concepts. Pediatr Investig. 2022; 6:123–34.
Article
2. Cavarzere P, Castanet M, Polak M, Raux-Demay MC, Cabrol S, Carel JC, et al. Clinical description of infants with congenital hypothyroidism and iodide organification defects. Horm Res. 2008; 70:240–8.
Article
3. Narumi S. Deciphering the mystery of CHNG3. Ann Pediatr Endocrinol Metab. 2024; 29:279–83.
Article
4. Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, et al. Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities. Nat Genet. 2024; 56:869–76.
Article
5. Ellegren H. Microsatellites: simple sequences with complex evolution. Nat Rev Genet. 2004; 5:435–45.
Article
6. Tóth G, Gáspári Z, Jurka J. Microsatellites in different eukaryotic genomes: survey and analysis. Genome Res. 2000; 10:967–81.
Article
7. Zhu H, Song P, Koo DH, Guo L, Li Y, Sun S, et al. Genome wide characterization of simple sequence repeats in watermelon genome and their application in comparative mapping and genetic diversity analysis. BMC Genomics. 2016; 17:557.
Article