APA (7th ed.) Citation

Weik, A. K., Rohrschneider, K., Strom, T. M., Glöckle, N., Kohl, S., Wissinger, B., & Weisschuh, N. (2016). Homozygosity mapping and whole-genome sequencing reveals a deep intronic PROM1 mutation causing cone-rod dystrophy by pseudoexon activation. European journal of human genetics, 24(3), . https://doi.org/10.1038/ejhg.2015.144

Chicago Style (17th ed.) Citation

Weik, Anja Kathrin, Klaus Rohrschneider, Tim M. Strom, Nicola Glöckle, Susanne Kohl, Bernd Wissinger, and Nicole Weisschuh. "Homozygosity Mapping and Whole-genome Sequencing Reveals a Deep Intronic PROM1 Mutation Causing Cone-rod Dystrophy by Pseudoexon Activation." European Journal of Human Genetics 24, no. 3 (2016). https://doi.org/10.1038/ejhg.2015.144.

MLA (9th ed.) Citation

Weik, Anja Kathrin, et al. "Homozygosity Mapping and Whole-genome Sequencing Reveals a Deep Intronic PROM1 Mutation Causing Cone-rod Dystrophy by Pseudoexon Activation." European Journal of Human Genetics, vol. 24, no. 3, 2016, https://doi.org/10.1038/ejhg.2015.144.