Scientists discover gene which causes rare disease in babies (EurekAlert, 29 May 2012)

30 May 2012


Researchers working at Queen Mary, University of London, have discovered mutations in a specific gene which may account for cases of Familial Glucocorticoid Deficiency (FGD). The research is published in Nature Genetics.

Full article


Related Topics

Adrenal Diabetes Metabolism Obesity Cardiovascular Bone Endocrine-Disrupting Chemicals Endocrine-Related Cancer Neuroendocrinology Reproduction Steroid and Steroidogenesis Thyroid

Share this story