Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing.

MLA

Tsai, Yu-Chih, et al. “Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing.” The Journal of Molecular Diagnostics : JMD, vol. 24, no. 11, Nov. 2022, pp. 1143–54. EBSCOhost, https://doi.org/10.1016/j.jmoldx.2022.08.003.

APA

Tsai, Y.-C., de Pontual, L., Heiner, C., Stojkovic, T., Furling, D., Bassez, G., Gourdon, G., & Tomé, S. (2022). Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing. The Journal of Molecular Diagnostics : JMD, 24(11), 1143–1154. https://doi.org/10.1016/j.jmoldx.2022.08.003

Chicago

Tsai, Yu-Chih, Laure de Pontual, Cheryl Heiner, Tanya Stojkovic, Denis Furling, Guillaume Bassez, Geneviève Gourdon, and Stéphanie Tomé. 2022. “Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read Sequencing.” The Journal of Molecular Diagnostics : JMD 24 (11): 1143–54. doi:10.1016/j.jmoldx.2022.08.003.