RF33 | PSAT69 A Combined Candidate Gene/Whole Exome Sequencing Approach Permits a Rapid Genetic Diagnosis for >81% Individuals with Primary Adrenal Insufficiency. (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/10.1210/jendso/bvac150.286
Publication URI: http://dx.doi.org/10.1210/jendso/bvac150.286
Type: Journal Article/Review
Parent Publication: Journal of the Endocrine Society
Issue: Supplement_1