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Updated: Feb 9, 2026

Characterizing Mutational Load and Clonal Composition of Human Blood
Published on: July 11, 2019
TRα Mutations in Human
C Briet1, Natacha Bouhours-Nouet1, F Illouz1
1Centre de référence des maladies rares de la thyroïde et des Récepteurs hormonaux, service EDN, CHU d'Angers, Institut MITOVASC, Université d'Angers, Angers, France.
Abstract:
Resistance to thyroid hormone alpha is an emerging syndrome, with up to now a limited number of published cases. Some features are common to most of the patients, but there is still some work to provide a comprehensive description of the full spectrum of the syndrome. A survey of the strategy to screen for and characterize the mutations in TR α gene is given.
Insights
Resistance to thyroid hormone alpha (TRα) is a rare syndrome with evolving characteristics. Further research is needed to fully define its spectrum and improve mutation detection strategies for the TRα gene.
Area of Science:
- Endocrinology
- Genetics
- Molecular Biology
Background:
- Resistance to thyroid hormone alpha (TRα) is an emerging clinical syndrome.
- Limited published cases exist, necessitating further characterization of its full spectrum.
- Understanding TRα resistance is crucial for diagnosing and managing affected individuals.
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