Eighteen-years follow-up of congenital hypothyroidism by TSHR gene p.Arg109Gln and p.Arg450His variants

Congenital hypothyroidism (CH) is a common heterogeneous endocrine disorder. The thyroid-stimulating hormone receptor gene (TSHR) is one of the major candidate genes associated with CH. Studies have investigated the possible correlations between the specific clinical features and the presence of TSH...

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Detalles Bibliográficos
Autores principales: Watanabe, Daisuke, Yagasaki, Hideaki, Mitsui, Yumiko, Inukai, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281846/
https://www.ncbi.nlm.nih.gov/pubmed/37346832
http://dx.doi.org/10.18999/nagjms.85.2.369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281846/
https://www.ncbi.nlm.nih.gov/pubmed/37346832
http://dx.doi.org/10.18999/nagjms.85.2.369

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