A Sphingosine-1-Phosphate Lyase Mutation Associated With Congenital Nephrotic Syndrome and Multiple Endocrinopathy. (2020)
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/10.3389/fped.2020.00151
PubMed Identifier: 32322566
Publication URI: http://europepmc.org/abstract/MED/32322566
Type: Journal Article/Review
Volume: 8
Parent Publication: Frontiers in pediatrics
ISSN: 2296-2360