A mutation in thioredoxin reductase 2 (TXNRD2) is associated with a predominantly adrenal phenotype in humans
Year: 2013
Type: conference-abstract
Source: Endocrine Abstracts
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Funder: Medical Research Council
OpenAlex ID: W2046442010
