de Feraudy, Y., Vandroux, M., Romero, N. B., Schneider, R., Saker, S., Boland, A., . . . Laporte, J. (2024). Exome sequencing in undiagnosed congenital myopathy reveals new genes and refines genes–phenotypes correlations. Genome Medicine, 16(1), 1. https://doi.org/10.1186/s13073-024-01353-0
Chicago Style (17th ed.) Citationde Feraudy, Yvan, et al. "Exome Sequencing in Undiagnosed Congenital Myopathy Reveals New Genes and Refines Genes–phenotypes Correlations." Genome Medicine 16, no. 1 (2024): 1. https://doi.org/10.1186/s13073-024-01353-0.
MLA (9th ed.) Citationde Feraudy, Yvan, et al. "Exome Sequencing in Undiagnosed Congenital Myopathy Reveals New Genes and Refines Genes–phenotypes Correlations." Genome Medicine, vol. 16, no. 1, 2024, p. 1, https://doi.org/10.1186/s13073-024-01353-0.