Research
Genetic origin of a rare form of Cushing’s syndrome finally identified
… the sequencing data, we identified a mutation in the KDM1A gene coding for lysine demethylase. It was therefore … of this event in macronodular adrenal hyperplasia.” An international collaboration to establish a patient cohort … The combination of the inherited germline mutation of KDM1A and the loss of the short arm of chromosome 1 in the …Published on: Thu 02/12/2021 - 17:38