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Further Evidence That Defects in Main Thyroid Dysgenesis-Related Genes Are an Uncommon Etiology for Primary Congenital Hypothyroidism in Mexican Patients: Report of Rare Variants in FOXE1, NKX2-5 and TSHR.
Children (Basel). 2021 May 30;8(6):457. doi: 10.3390/children8060457.
Children (Basel). 2021.
PMID: 34070861
Free PMC article.
Gene Variants in NKX2-1 Do Not Represent a Major Etiological Factor of Primary Congenital Hypothyroidism in Mexican Population.
González-Del Angel A, Fernández-Hernández L, Sánchez-Verdiguel I, González-Núñez A, Martínez-Cruz V, Sánchez C, Moreno-Rojas R, Alcántara-Ortigoza MA.
González-Del Angel A, et al. Among authors: sanchez verdiguel i.
J Pediatr Genet. 2019 Jun;8(2):41-46. doi: 10.1055/s-0038-1676644. Epub 2019 Jan 2.
J Pediatr Genet. 2019.
PMID: 31061744
Free PMC article.
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