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Updated: Nov 2, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing

Aryel Furman1, Zeina Hannoush1, Francisco Barrera Echegoyen1

  • 1Department of Medicine; University of Miami Miller School of Medicine, Miami, Florida, USA.

Thyroid : Official Journal of the American Thyroid Association
|June 15, 2021
PubMed

Keywords:
congenital hypothyroidismdeiodinasereverse T3thyroperoxidase

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