Gene Variants in NKX2-1 Do Not Represent a Major Etiological Factor of Primary Congenital Hypothyroidism in Mexican Population

Congenital hypothyroidism (CH), attributable to thyroid dysgenesis (TD), has an unusually high prevalence in Mexican population but the causes are unknown. NKX2-1 , as a candidate gene, was subjected to automated Sanger sequencing in 122 unrelated Mexican patients with CH/TD. Although this study inc...

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Veröffentlicht in:J Pediatr Genet
Hauptverfasser: González-del Angel, Ariadna, Fernández-Hernández, Liliana, Sánchez-Verdiguel, Iraís, González-Núñez, Aidy, Martínez-Cruz, Víctor, Sánchez, Carmen, Moreno-Rojas, Rosario, Alcántara-Ortigoza, Miguel Angel
Format: Artigo
Sprache:Inglês
Veröffentlicht: Georg Thieme Verlag KG 2019
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6499623/
https://ncbi.nlm.nih.gov/pubmed/31061744
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0038-1676644
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