Cargando…
Association of TSHR gene single nucleotide intronic polymorphism with the risk of hypothyroid and hyperthyroid disorders in Yazd province
The present study was carried out, for the first time, to evaluate the association of rs2268458 polymorphism, biochemical and environmental factors on hypothyroid and hyperthyroid disorders in thyroid patients and healthy individuals in Yazd province, Iran. In this study, blood samples were collecte...
Autores principales: | Naghibi, Fahime Sadat, Miresmaeili, Seyed Mohsen, Javid, Amaneh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9492782/ https://www.ncbi.nlm.nih.gov/pubmed/36130976 http://dx.doi.org/10.1038/s41598-022-19822-0 |
Ejemplares similares
-
Correlation of TSHR and CTLA-4 Single Nucleotide Polymorphisms with Graves Disease
por: Sun, Weihua, et al.
Publicado: (2019) -
Molecular investigation of TSHR gene in Bangladeshi congenital hypothyroid patients
por: Begum, Mst. Noorjahan, et al.
Publicado: (2023) -
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
por: Cho, Won Kyoung, et al.
Publicado: (2018) -
Hypothyroidism and hyperthyroidism
por: Guerri, Giulia, et al.
Publicado: (2019) -
Prevalence of Neonatal Hyperphenylalaninemia in Yazd Province, Iran
por: Ordooei, Mahtab, et al.
Publicado: (2015)