Frequency of UCP2 45-bp Ins/Del polymorphism in Saudi population from Jazan area and its association with autoimmune hypothyroidism UCP2 45-bp Ins/Del frequency in hypothyroidism

OBJECTIVES: Autoimmune hypothyroidism (AHT) is a common endocrine disorder. Although the exact cause of AHT is not yet understood, genetic factors may play a major role. Uncoupling protein 2 (UCP2) is a member of mitochondrial protein family involved in the regulation of cellular metabolism. An impo...

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Publicat a:Int J Health Sci (Qassim)
Autors principals: Kaabi, Yahia A., Mansor, Abdullah S., Alfagih, Ashwag S., Hakami, Alhussain M., Summ, Mohammed A., Mjery, Yahia A., Alzughbi, Mona N., Habibullah, Mahmoud M.
Format: Artigo
Idioma:Inglês
Publicat: Qassim Uninversity 2020
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7346973/
https://ncbi.nlm.nih.gov/pubmed/32694967
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