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Identification and characterization of novel PAX8 mutations in Congenital Hypothyroidism(CH) in a Chinese population
OBJECTIVE: Based on mutations in PAX8 is associated with thyroid dysgenesis. We aim to identify and characterize PAX8 mutations in a large cohort of congenital hypothyroidism(CH) from thyroid dysgenesis in Chinese population. METHODS: We screened 453 unrelated Chinese patients with CH from thyroid d...
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| Udgivet i: | Oncotarget |
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| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Impact Journals LLC
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5352434/ https://ncbi.nlm.nih.gov/pubmed/28060725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.14419 |
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