Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. (2014)

First Author: Handley MT
Attributed to:  Genetic models of human disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mgg3.70

PubMed Identifier: 25077174

Publication URI: http://europepmc.org/abstract/MED/25077174

Type: Journal Article/Review

Volume: 2

Parent Publication: Molecular genetics & genomic medicine

Issue: 4

ISSN: 2324-9269