Xie, W., Liao, B., Shuai, M., Liu, R., Hong, M., & He, S. (2025). Novel De Novo Intronic Variant of SYNGAP1 Associated With the Neurodevelopmental Disorders. Molecular Genetics & Genomic Medicine, 13(2), . https://doi.org/10.1002/mgg3.70066
Chicago Style (17th ed.) CitationXie, Wuming, Baoqiong Liao, Mei Shuai, Rutian Liu, Min Hong, and Shuwen He. "Novel De Novo Intronic Variant of SYNGAP1 Associated With the Neurodevelopmental Disorders." Molecular Genetics & Genomic Medicine 13, no. 2 (2025). https://doi.org/10.1002/mgg3.70066.
MLA (9th ed.) CitationXie, Wuming, et al. "Novel De Novo Intronic Variant of SYNGAP1 Associated With the Neurodevelopmental Disorders." Molecular Genetics & Genomic Medicine, vol. 13, no. 2, 2025, https://doi.org/10.1002/mgg3.70066.