Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism

Congenital primary hypothyroidism (CH; OMIM 218700) is characterized by an impaired thyroid development, or dyshormonogenesis, and can lead to intellectual disability and growth retardation if untreated. Most of the children with congenital hypothyroidism present thyroid dysgenesis, a developmental...

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Detalles Bibliográficos
Autores principales: Vick, Philipp, Eberle, Birgit, Choukair, Daniela, Weiss, Birgit, Roeth, Ralph, Schneider, Isabelle, Paramasivam, Nagarajan, Bettendorf, Markus, Rappold, Gudrun A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701029/
https://www.ncbi.nlm.nih.gov/pubmed/34946811
http://dx.doi.org/10.3390/genes12121862

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701029/
https://www.ncbi.nlm.nih.gov/pubmed/34946811
http://dx.doi.org/10.3390/genes12121862

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