APA (7th ed.) Citation

Metay, C., Ghanem, R., Toutain, A., Bloch, A., Blin, E., Jobic, V., . . . Richard, P. (2024). 16P Limitation of short-reads NGS sequencing on genomic DNA: Interest of functional studies in the diagnosis of congenital Ullrich muscular dystrophy. Neuromuscular Disorders, 43, N.PAG. https://doi.org/10.1016/j.nmd.2024.07.223

Chicago Style (17th ed.) Citation

Metay, C., et al. "16P Limitation of Short-reads NGS Sequencing on Genomic DNA: Interest of Functional Studies in the Diagnosis of Congenital Ullrich Muscular Dystrophy." Neuromuscular Disorders 43 (2024): N.PAG. https://doi.org/10.1016/j.nmd.2024.07.223.

MLA (9th ed.) Citation

Metay, C., et al. "16P Limitation of Short-reads NGS Sequencing on Genomic DNA: Interest of Functional Studies in the Diagnosis of Congenital Ullrich Muscular Dystrophy." Neuromuscular Disorders, vol. 43, 2024, p. N.PAG, https://doi.org/10.1016/j.nmd.2024.07.223.