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-referens (17:e uppl.)Handley, Mark T., André Mégarbané, Alison M. Meynert, Stephen Brown, Elisabeth Freyer, Martin S. Taylor, Ian J. Jackson, och 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-referens (9:e uppl.)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.
