Maugeri, A., Driel, M. A. v., Pol, D. J. R. v. d., Klevering, B. J., Haren, F. J. J. v., Tijmes, N., . . . Cremers, F. P. M. (1999). The 2588G→C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease. The American journal of human genetics, 64(4), . https://doi.org/10.1086/302323
Chicago-Zitierstil (17. Ausg.)Maugeri, Alessandra, et al. "The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease." The American Journal of Human Genetics 64, no. 4 (1999). https://doi.org/10.1086/302323.
MLA-Zitierstil (9. Ausg.)Maugeri, Alessandra, et al. "The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease." The American Journal of Human Genetics, vol. 64, no. 4, 1999, https://doi.org/10.1086/302323.