Defective erythropoiesis caused by mutations of the thyroid hormone receptor α gene.

Patients with mutations of the THRA gene exhibit classical features of hypothyroidism, including erythroid disorders. We previously created a mutant mouse expressing a mutated TRα1 (denoted as PV; Thra1PV/+ mouse) that faithfully reproduces the classical hypothyroidism seen in patients. Using Thra1P...

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Autors principals:	Sunmi Park, Cho Rong Han, Jeong Won Park, Li Zhao, Xuguang Zhu, Mark Willingham, David M Bodine, Sheue-Yann Cheng
Format:	Artigo
Idioma:	Inglês
Publicat:	Public Library of Science (PLoS) 2017-09-01
Col·lecció:	PLoS Genetics
Accés en línia:	https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1006991&type=printable
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