Related Articles
Mutation spectrum analysis of 29 causative genes in 43 Chinese patients with congenital hypothyroidism
MicroRNA‑1236‑3p/translationally controlled tumor protein (TPT1) axis participates in congenital hypothyroidism progression by regulating neuronal apoptosis
Mutation and expression of ABCA12 in keratosis pilaris and nevus comedonicus
MicroRNA‑489‑3p plays a significant role in congenital hypothyroidism through regulating neuronal cell apoptosis via targeting translationally controlled tumor protein 1
A novel frameshift mutation in the <em>FERMT1</em> gene in a Chinese patient with Kindler syndrome