Copelli, M.d.M.; Pairet, E.; Atique-Tacla, M.; Vieira, T.P.; Appenzeller, S.; Helaers, R.; Vikkula, M.; Gil-da-Silva-Lopes, V.L.
SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes 2023, 14, 882.
https://doi.org/10.3390/genes14040882
AMA Style
Copelli MdM, Pairet E, Atique-Tacla M, Vieira TP, Appenzeller S, Helaers R, Vikkula M, Gil-da-Silva-Lopes VL.
SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes. 2023; 14(4):882.
https://doi.org/10.3390/genes14040882
Chicago/Turabian Style
Copelli, Matheus de Mello, Eleonore Pairet, Milena Atique-Tacla, Társis Paiva Vieira, Simone Appenzeller, Raphaël Helaers, Miikka Vikkula, and Vera Lúcia Gil-da-Silva-Lopes.
2023. "SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review" Genes 14, no. 4: 882.
https://doi.org/10.3390/genes14040882
APA Style
Copelli, M. d. M., Pairet, E., Atique-Tacla, M., Vieira, T. P., Appenzeller, S., Helaers, R., Vikkula, M., & Gil-da-Silva-Lopes, V. L.
(2023). SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review. Genes, 14(4), 882.
https://doi.org/10.3390/genes14040882