A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencing.

MLA

Nabavizadeh, Nasrinsadat, et al. “A Progeroid Syndrome Caused by a Deep Intronic Variant in TAPT1 Is Revealed by RNA/SI-NET Sequencing.” EMBO Molecular Medicine, vol. 15, no. 2, Feb. 2023, p. e16478. EBSCOhost, https://doi.org/10.15252/emmm.202216478.

APA

Nabavizadeh, N., Bressin, A., Shboul, M., Moreno Traspas, R., Chia, P. H., Bonnard, C., Szenker-Ravi, E., Sarıbaş, B., Beillard, E., Altunoglu, U., Hojati, Z., Drutman, S., Freier, S., El-Khateeb, M., Fathallah, R., Casanova, J.-L., Soror, W., Arafat, A., Escande-Beillard, N., … Reversade, B. (2023). A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencing. EMBO Molecular Medicine, 15(2), e16478. https://doi.org/10.15252/emmm.202216478

Chicago

Nabavizadeh, Nasrinsadat, Annkatrin Bressin, Mohammad Shboul, Ricardo Moreno Traspas, Poh Hui Chia, Carine Bonnard, Emmanuelle Szenker-Ravi, et al. 2023. “A Progeroid Syndrome Caused by a Deep Intronic Variant in TAPT1 Is Revealed by RNA/SI-NET Sequencing.” EMBO Molecular Medicine 15 (2): e16478. doi:10.15252/emmm.202216478.