Itai, T., Hamanaka, K., Sasaki, K., Wagner, M., Kotzaeridou, U., Brösse, I., . . . Matsumoto, N. (2021). De novo variants in CELF2 that disrupt the nuclear localization signal cause developmental and epileptic encephalopathy. Human mutation, 42(1), . https://doi.org/https://doi.org/10.1002/humu.24130
Chicago-Zitierstil (17. Ausg.)Itai, Toshiyuki, et al. "De Novo Variants in CELF2 That Disrupt the Nuclear Localization Signal Cause Developmental and Epileptic Encephalopathy." Human Mutation 42, no. 1 (2021). https://doi.org/https://doi.org/10.1002/humu.24130.
MLA-Zitierstil (9. Ausg.)Itai, Toshiyuki, et al. "De Novo Variants in CELF2 That Disrupt the Nuclear Localization Signal Cause Developmental and Epileptic Encephalopathy." Human Mutation, vol. 42, no. 1, 2021, https://doi.org/https://doi.org/10.1002/humu.24130.