Bernal Barquero, C.E.; Geysels, R.C.; Jacques, V.; Carro, G.H.; MartÃn, M.; Peyret, V.; Abregú, M.C.; Papendieck, P.; Masini-Repiso, A.M.; Savagner, F.;
et al. Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect. Int. J. Mol. Sci. 2022, 23, 9251.
https://doi.org/10.3390/ijms23169251
AMA Style
Bernal Barquero CE, Geysels RC, Jacques V, Carro GH, MartÃn M, Peyret V, Abregú MC, Papendieck P, Masini-Repiso AM, Savagner F,
et al. Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect. International Journal of Molecular Sciences. 2022; 23(16):9251.
https://doi.org/10.3390/ijms23169251
Chicago/Turabian Style
Bernal Barquero, Carlos Eduardo, Romina Celeste Geysels, Virginie Jacques, Gerardo Hernán Carro, Mariano MartÃn, Victoria Peyret, MarÃa Celeste Abregú, Patricia Papendieck, Ana MarÃa Masini-Repiso, Frédérique Savagner,
and et al. 2022. "Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect" International Journal of Molecular Sciences 23, no. 16: 9251.
https://doi.org/10.3390/ijms23169251
APA Style
Bernal Barquero, C. E., Geysels, R. C., Jacques, V., Carro, G. H., MartÃn, M., Peyret, V., Abregú, M. C., Papendieck, P., Masini-Repiso, A. M., Savagner, F., Chiesa, A. E., Citterio, C. E., & Nicola, J. P.
(2022). Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect. International Journal of Molecular Sciences, 23(16), 9251.
https://doi.org/10.3390/ijms23169251
