Handley, M. T., Mégarbané, A., Meynert, A. M., Brown, S., Freyer, E., Taylor, M. S., . . . Aligianis, I. A. (2014, July). 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.
芝加哥风格引文Handley, Mark T., André Mégarbané, Alison M. Meynert, Stephen Brown, Elisabeth Freyer, Martin S. Taylor, Ian J. Jackson, 与 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 Jul. 2014.
MLA引文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, Jul. 2014.