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Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism
Primary congenital hypothyroidism (CH) is a common neonatal endocrine disorder characterized by elevated concentrations of thyroid stimulating hormone (TSH) and low concentrations of free thyroxine (FT4). PAX8 and NKX2-1 are important transcription factors involved in thyroid development. In this st...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821711/ https://www.ncbi.nlm.nih.gov/pubmed/36614229 http://dx.doi.org/10.3390/ijms24010786 |