Evers, C., Paramasivam, N., Hinderhofer, K., Fischer, C., Granzow, M., Schmidt-Bacher, A., . . . Moog, U. (2015). SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract. European journal of human genetics, 23(12), . https://doi.org/10.1038/ejhg.2015.46
Chicago-Zitierstil (17. Ausg.)Evers, Christina, et al. "SIPA1L3 Identified by Linkage Analysis and Whole-exome Sequencing as a Novel Gene for Autosomal Recessive Congenital Cataract." European Journal of Human Genetics 23, no. 12 (2015). https://doi.org/10.1038/ejhg.2015.46.
MLA-Zitierstil (9. Ausg.)Evers, Christina, et al. "SIPA1L3 Identified by Linkage Analysis and Whole-exome Sequencing as a Novel Gene for Autosomal Recessive Congenital Cataract." European Journal of Human Genetics, vol. 23, no. 12, 2015, https://doi.org/10.1038/ejhg.2015.46.