New genetics in congenital hypothyroidism.

Athanasia StoupaDulanjalee KariyawasamMarina MuzzaTiziana de FilippisLaura FugazzolaMichel PolakLuca PersaniAurore Carré

Published in: Endocrine (2021)

We provide an overview of recent genetic causes of primary and central CH. In addition, mode of inheritance and the oligogenic model of CH are discussed.

Keyphrases

room temperature
mitochondrial dna
copy number
genome wide
replacement therapy
dna methylation