A, M., E, P., S, Y., A, L., H, M., T, G., . . . T, H. (2023). A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delay. Clinical genetics, 104(1), 73. https://doi.org/10.1111/cge.14335
Chicago Style (17th ed.) CitationA, Mo, et al. "A Recurrent De Novo Variant in NUSAP1 Escapes Nonsense-mediated Decay and Leads to Microcephaly, Epilepsy, and Developmental Delay." Clinical Genetics 104, no. 1 (2023): 73. https://doi.org/10.1111/cge.14335.
MLA (9th ed.) CitationA, Mo, et al. "A Recurrent De Novo Variant in NUSAP1 Escapes Nonsense-mediated Decay and Leads to Microcephaly, Epilepsy, and Developmental Delay." Clinical Genetics, vol. 104, no. 1, 2023, p. 73, https://doi.org/10.1111/cge.14335.
Warning: These citations may not always be 100% accurate.
