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Amedeo Smart

Independent Medical Education


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Furman AE, Hannoush Z, Barrera Echegoyen FX, Dumitrescu AM, et al. Novel DIO1 gene mutation acting as phenotype modifier for novel compound heterozygous TPO gene mutations causing congenital hypothyroidism. Thyroid 2021 Jun 15. doi: 10.1089/thy.2021.0210.
PMID: 34128397


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