Extended clinical features associated with novel Glis3 mutation: a case report

Mutations in the GLI-similar 3 (GLIS3) gene encoding the transcription factor GLIS3 are a rare cause of neonatal diabetes and congenital hypothyroidism with 12 reported patients to date. Additional features, p...

Source: BMC Endocrine Disorders - March 2, 2017 Category: Endocrinology Authors: K. A. Alghamdi, A. B. Alsaedi, A. Aljasser, A. Altawil and Naglaa M. Kamal Source Type: research