APA (7th ed.) Citation

Handley, M. T., Mégarbané, A., Meynert, A. M., Brown, S., Freyer, E., Taylor, M. S., . . . Aligianis, I. A. (2014). 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, 2(4), 319. https://doi.org/10.1002/mgg3.70

Chicago Style (17th ed.) Citation

Handley, Mark T., André Mégarbané, Alison M. Meynert, Stephen Brown, Elisabeth Freyer, Martin S. Taylor, Ian J. Jackson, and Irene A. Aligianis. "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 2, no. 4 (2014): 319. https://doi.org/10.1002/mgg3.70.

MLA (9th ed.) Citation

Handley, Mark T., et al. "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, vol. 2, no. 4, 2014, p. 319, https://doi.org/10.1002/mgg3.70.