A rapid genetic diagnosis for >80% individuals with non-CAH Primary Adrenal Insufficiency is achievable by candidate gene sequencing combined with WES (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.81.rc2.1
Publication URI: http://dx.doi.org/10.1530/endoabs.81.rc2.1
Type: Journal Article/Review
Parent Publication: Endocrine Abstracts