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A De novo PAX8 mutation in a Chinese child with congenital thyroid dysgenesis
Background: Thyroid dysgenesis (TD) is the most frequent cause of congenital hypothyroidism (CH), but its pathogenesis remains unclear. As a thyroid transcription factor, paired box transcription factor 8 (PAX8) is essential for thyroid organogenesis and development. Aim: To screen PAX8 mutations an...
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| Publicado no: | Int J Clin Exp Pathol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
e-Century Publishing Corporation
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4637687/ https://ncbi.nlm.nih.gov/pubmed/26617871 |
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