APA (7th ed.) Citation

Ruan, D., Ruan, X., Wang, R., Lin, X., Zhang, Y., Lin, B., . . . Li, Y. (2024). Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation. Scientific Reports, 14(1), 1. https://doi.org/10.1038/s41598-024-58452-6

Chicago Style (17th ed.) Citation

Ruan, Dan-dan, et al. "Clinical Phenotype and Genetic Function Analysis of a Family with Hypomyelinating Leukodystrophy-7 Caused by POLR3A Mutation." Scientific Reports 14, no. 1 (2024): 1. https://doi.org/10.1038/s41598-024-58452-6.

MLA (9th ed.) Citation

Ruan, Dan-dan, et al. "Clinical Phenotype and Genetic Function Analysis of a Family with Hypomyelinating Leukodystrophy-7 Caused by POLR3A Mutation." Scientific Reports, vol. 14, no. 1, 2024, p. 1, https://doi.org/10.1038/s41598-024-58452-6.