Holtz, A. M., VanCoillie, R., Vansickle, E. A., Carere, D. A., Withrow, K., Torti, E., . . . Raby, B. A. (2022). Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. Genetics in medicine, 24(10), . https://doi.org/10.1016/j.gim.2022.07.005
Chicago-Zitierstil (17. Ausg.)Holtz, Alexander M., et al. "Heterozygous Variants in MYH10 Associated with Neurodevelopmental Disorders and Congenital Anomalies with Evidence for Primary Cilia-dependent Defects in Hedgehog Signaling." Genetics in Medicine 24, no. 10 (2022). https://doi.org/10.1016/j.gim.2022.07.005.
MLA-Zitierstil (9. Ausg.)Holtz, Alexander M., et al. "Heterozygous Variants in MYH10 Associated with Neurodevelopmental Disorders and Congenital Anomalies with Evidence for Primary Cilia-dependent Defects in Hedgehog Signaling." Genetics in Medicine, vol. 24, no. 10, 2022, https://doi.org/10.1016/j.gim.2022.07.005.