Investigation of the impact of nonsynonymous mutations on thyroid peroxidase dimer
Our genetics research team has recently published a paper on congenital hypothyroidism entitled,” Investigation of the impact of nonsynonymous mutations on thyroid peroxidase dimer”. This paper highlights Thyroid Dyshormonogenesis, hereditary defects in thyroid hormone synthesis and secretion. Thyroid peroxidase dimer protein plays a major role in thyroid hormone synthesis. Nonsynonymous mutations on Thyroid Peroxidase (TPO) […]
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