Cite
High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations.
MLA
Rath, Matthias, et al. “High-Throughput Sequencing of the Entire Genomic Regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to Search for Pathogenic Deep-Intronic Splice Mutations in Cerebral Cavernous Malformations.” European Journal of Medical Genetics, vol. 60, no. 9, Sept. 2017, pp. 479–84. EBSCOhost, https://doi.org/10.1016/j.ejmg.2017.06.007.
APA
Rath, M., Jenssen, S. E., Schwefel, K., Spiegler, S., Kleimeier, D., Sperling, C., Kaderali, L., & Felbor, U. (2017). High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations. European Journal of Medical Genetics, 60(9), 479–484. https://doi.org/10.1016/j.ejmg.2017.06.007
Chicago
Rath, Matthias, Sönke E. Jenssen, Konrad Schwefel, Stefanie Spiegler, Dana Kleimeier, Christian Sperling, Lars Kaderali, and Ute Felbor. 2017. “High-Throughput Sequencing of the Entire Genomic Regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to Search for Pathogenic Deep-Intronic Splice Mutations in Cerebral Cavernous Malformations.” European Journal of Medical Genetics 60 (9): 479–84. doi:10.1016/j.ejmg.2017.06.007.