APA

Handley M. T., Mégarbané A., Meynert A. M., Brown S., Freyer E., Taylor M. S., Jackson I. J. & Aligianis I. A. (20140731). 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. : Molecular genetics & genomic medicine.

Chicago

Handley Mark T, Mégarbané André, Meynert Alison M, Brown Stephen, Freyer Elisabeth, Taylor Martin S, Jackson Ian J and Aligianis Irene A. 20140731. 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. : Molecular genetics & genomic medicine.

Harvard

Handley M. T., Mégarbané A., Meynert A. M., Brown S., Freyer E., Taylor M. S., Jackson I. J. and Aligianis I. A. (20140731). 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. : Molecular genetics & genomic medicine.

MLA

Handley Mark T, Mégarbané André, Meynert Alison M, Brown Stephen, Freyer Elisabeth, Taylor Martin S, Jackson Ian J and Aligianis Irene A. 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. : Molecular genetics & genomic medicine. 20140731.