Opladen, T., Sengupta, D., Moog, U., Fischer, C., Bürger, F., Haas, D., . . . Hoffmann, G. F. (2014). Aspartylglucosaminuria: Unusual neonatal presentation in qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family. Journal of child neurology, 29(1), . https://doi.org/10.1177/0883073812469049
Chicago-Zitierstil (17. Ausg.)Opladen, Thomas, Devjani Sengupta, Ute Moog, Christine Fischer, Friederike Bürger, Dorothea Haas, Inga Harting, und Georg F. Hoffmann. "Aspartylglucosaminuria: Unusual Neonatal Presentation in Qatari Twins with a Novel Aspartylglucosaminidase Gene Mutation and 3 New Cases in a Turkish Family." Journal of Child Neurology 29, no. 1 (2014). https://doi.org/10.1177/0883073812469049.
MLA-Zitierstil (9. Ausg.)Opladen, Thomas, et al. "Aspartylglucosaminuria: Unusual Neonatal Presentation in Qatari Twins with a Novel Aspartylglucosaminidase Gene Mutation and 3 New Cases in a Turkish Family." Journal of Child Neurology, vol. 29, no. 1, 2014, https://doi.org/10.1177/0883073812469049.