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Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis
OBJECTIVE: Congenital hypothyroidism (CH) is a frequent neonatal endocrine disease with an incidence of about 1:2500 worldwide. Although thyroid dysgenesis (TD) is the most frequent cause of CH cases, its pathogenesis remains unclear. The aim of this study was to screen the hematopoietically-express...
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| Vydáno v: | J Clin Res Pediatr Endocrinol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Galenos Publishing
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805044/ https://ncbi.nlm.nih.gov/pubmed/26757609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.2456 |
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