Recurrent "outsider" intronic variation in the SLC5A 6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb.

MLA

Mansour-Hendili, Lamisse, et al. “Recurrent ‘Outsider’ Intronic Variation in the SLC5A 6 Gene Causes Severe Mixed Axonal and Demyelinating Neuropathy, Cyclic Vomiting and Optic Atrophy in 3 Families from Maghreb.” Frontiers in Genetics, vol. 15, Jan. 2024, p. 1352006. EBSCOhost, https://doi.org/10.3389/fgene.2024.1352006.

APA

Mansour-Hendili, L., Gitiaux, C., Harion, M., Latouche, C., Heron, B., Stojkovic, T., Rama, M., Smol, T., Sophie Jourdain, A., Mention, K., Nadjar, Y., Schiff, M., Lemale, J., Ghoumid, J., Gottrand, F., Talbotec, C., Rötig, A., Funalot, B., & Desguerre, I. (2024). Recurrent “outsider” intronic variation in the SLC5A 6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb. Frontiers in Genetics, 15, 1352006. https://doi.org/10.3389/fgene.2024.1352006

Chicago

Mansour-Hendili, Lamisse, Cyril Gitiaux, Madeleine Harion, Céline Latouche, Bénédicte Heron, Tanya Stojkovic, Mélanie Rama, et al. 2024. “Recurrent ‘Outsider’ Intronic Variation in the SLC5A 6 Gene Causes Severe Mixed Axonal and Demyelinating Neuropathy, Cyclic Vomiting and Optic Atrophy in 3 Families from Maghreb.” Frontiers in Genetics 15 (January): 1352006. doi:10.3389/fgene.2024.1352006.