IGSF1 MUTATIONS ARE THE MOST FREQUENT GENETIC AETIOLOGY OF THYROTROPIN DEFICIENCY. Fourneaux R, Reynaud R, Mougel G, Castets S, et al. Eur J Endocrinol 2022 Oct 1. pii: EJE-22-0520. doi: 10.1530/EJE-22-0520.

Read + Share

Amedeo Smart

Independent Medical Education

Fourneaux R, Reynaud R, Mougel G, Castets S, et al. IGSF1 MUTATIONS ARE THE MOST FREQUENT GENETIC AETIOLOGY OF THYROTROPIN DEFICIENCY. Eur J Endocrinol 2022 Oct 1. pii: EJE-22-0520. doi: 10.1530/EJE-22-0520.
PMID: 36201163