Clinical and genetic features of luscan-lumish syndrome associated with a novel de novo variant of SETD2 gene: Case report and literature review.

MLA

Yanqing Zhang, et al. “Clinical and Genetic Features of Luscan-Lumish Syndrome Associated with a Novel de Novo Variant of SETD2 Gene: Case Report and Literature Review.” Frontiers in Genetics, vol. 14, Jan. 2023, pp. 1–7. EBSCOhost, https://doi.org/10.3389/fgene.2023.1081391.

APA

Yanqing Zhang, Haozheng Zhang, Wei Wu, Dong Wang, Yuqiang Lv, Dongmei Zhao, Lingxiao Wang, Yi Liu, & Kaihui Zhang. (2023). Clinical and genetic features of luscan-lumish syndrome associated with a novel de novo variant of SETD2 gene: Case report and literature review. Frontiers in Genetics, 14, 1–7. https://doi.org/10.3389/fgene.2023.1081391

Chicago

Yanqing Zhang, Haozheng Zhang, Wei Wu, Dong Wang, Yuqiang Lv, Dongmei Zhao, Lingxiao Wang, Yi Liu, and Kaihui Zhang. 2023. “Clinical and Genetic Features of Luscan-Lumish Syndrome Associated with a Novel de Novo Variant of SETD2 Gene: Case Report and Literature Review.” Frontiers in Genetics 14 (January): 1–7. doi:10.3389/fgene.2023.1081391.