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A Sphingosine-1-Phosphate Lyase Mutation Associated With Congenital Nephrotic Syndrome and Multiple Endocrinopathy. (2020)

First Author: Maharaj A

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