Genotype-phenotype association and functional analysis of hnRNPA1 mutations in amyotrophic lateral sclerosis.

MLA

Zhang, Xinyi, et al. “Genotype-Phenotype Association and Functional Analysis of HnRNPA1 Mutations in Amyotrophic Lateral Sclerosis.” Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, vol. 25, no. 5/6, Aug. 2024, pp. 600–07. EBSCOhost, https://doi.org/10.1080/21678421.2024.2346502.

APA

Zhang, X., Sun, Y., Zhang, X., Shen, D., Shu, S., Yang, X., Liu, M., Cui, L., Liu, Q., & Zhang, X. (2024). Genotype-phenotype association and functional analysis of hnRNPA1 mutations in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 25(5/6), 600–607. https://doi.org/10.1080/21678421.2024.2346502

Chicago

Zhang, Xinyi, Ye Sun, Xinzhe Zhang, Dongchao Shen, Shi Shu, Xunzhe Yang, Mingsheng Liu, Liying Cui, Qing Liu, and Xue Zhang. 2024. “Genotype-Phenotype Association and Functional Analysis of HnRNPA1 Mutations in Amyotrophic Lateral Sclerosis.” Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration 25 (5/6): 600–607. doi:10.1080/21678421.2024.2346502.