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The lack of genotype: phenotype correlations in rare causes of primary adrenal insufficiency highlights the need for genetic testing (2022)

First Author: Maitra S

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