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Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism
CONTEXT: Congenital hypothyroidism (CH) is due to dyshormonogenesis in 10% to 15% of subjects worldwide but accounts for 60% of CH cases in the Sudan. OBJECTIVE: To investigate the molecular basis of CH in Sudanese families. DESIGN: Clinical phenotype reporting and serum thyroid hormone measurements...
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| Publicat a: | J Clin Endocrinol Metab |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7093074/ https://ncbi.nlm.nih.gov/pubmed/31867598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/clinem/dgz297 |
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