Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies.

MLA

Salih, Mustafa A., et al. “Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies.” Genetic Testing and Molecular Biomarkers, vol. 25, no. 12, Dec. 2021, pp. 757–64. EBSCOhost, https://doi.org/10.1089/gtmb.2021.0085.

APA

Salih, M. A., Hamad, M. H., Savarese, M., Alorainy, I. A., Al-Jarallah, A. S., Alkhalidi, H., AlQudairy, H., Albader, A., Alotaibi, A. J., Alsagob, M., Al-Bakheet, A., Colak, D., Udd, B., & Kaya, N. (2021). Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies. Genetic Testing and Molecular Biomarkers, 25(12), 757–764. https://doi.org/10.1089/gtmb.2021.0085

Chicago

Salih, Mustafa A, Muddathir H Hamad, Marco Savarese, Ibrahim A Alorainy, Abdullah S Al-Jarallah, Hisham Alkhalidi, Hanan AlQudairy, et al. 2021. “Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies.” Genetic Testing and Molecular Biomarkers 25 (12): 757–64. doi:10.1089/gtmb.2021.0085.