The lack of genotype: phenotype correlations in rare causes of primary adrenal insufficiency highlights the need for genetic testing (2022)
Attributed to:
Deciphering mechanisms of disease associated with Sphingosine-1-phosphate lyase deficiency
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1530/endoabs.85.oc5.5
Publication URI: http://dx.doi.org/10.1530/endoabs.85.oc5.5
Type: Journal Article/Review
Parent Publication: Endocrine Abstracts