Cite
APA Citation
Lefebvre, M., Beaufrere, A., Francannet, C., Laurichesse, H., Poe, C., Jouan, T., Troude, B., Dechelotte, P., Vabres, P., Biard, M., Mosca‐Boidron, A., Duffourd, Y., Faivre, L., Thevenon, J., & Thauvin‐Robinet, C. (2018). extending the ALDH18A1 clinical spectrum to severe autosomal recessive fetal cutis laxa with corpus callosum agenesis. American journal of medical genetics, 176(11), 2509–2512. http://access.bl.uk/ark:/81055/vdc_100090658751.0x00002a