von Wrede, R.; Schidlowski, M.; Huppertz, H.-J.; Rüber, T.; Ivo, A.; Baumgartner, T.; Hallmann, K.; Zsurka, G.; Helmstaedter, C.; Surges, R.;
et al. Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes 2022, 13, 429.
https://doi.org/10.3390/genes13030429
AMA Style
von Wrede R, Schidlowski M, Huppertz H-J, Rüber T, Ivo A, Baumgartner T, Hallmann K, Zsurka G, Helmstaedter C, Surges R,
et al. Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes. 2022; 13(3):429.
https://doi.org/10.3390/genes13030429
Chicago/Turabian Style
von Wrede, Randi, Martin Schidlowski, Hans-Jürgen Huppertz, Theodor Rüber, Anja Ivo, Tobias Baumgartner, Kerstin Hallmann, Gábor Zsurka, Christoph Helmstaedter, Rainer Surges,
and et al. 2022. "Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits" Genes 13, no. 3: 429.
https://doi.org/10.3390/genes13030429
APA Style
von Wrede, R., Schidlowski, M., Huppertz, H.-J., Rüber, T., Ivo, A., Baumgartner, T., Hallmann, K., Zsurka, G., Helmstaedter, C., Surges, R., & Kunz, W. S.
(2022). Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes, 13(3), 429.
https://doi.org/10.3390/genes13030429
