Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene.

MLA

Sinkó, Gabriella, et al. “Vanishing White Matter Disease, a Rare Leukodystrophy with Mutation in the EIF2B5 Gene.” Clinical Neuroscience / Ideggyógyászati Szemle, vol. 77, no. 5/6, May 2024, pp. 207–11. EBSCOhost, https://doi.org/10.18071/isz.77.0207.

APA

Sinkó, G., Tompa, M., Kiss, Z., & Kálmán, B. (2024). Vanishing white matter disease, a rare leukodystrophy with mutation in the EIF2B5 gene. Clinical Neuroscience / Ideggyógyászati Szemle, 77(5/6), 207–211. https://doi.org/10.18071/isz.77.0207

Chicago

Sinkó, Gabriella, Márton Tompa, Zsuzsanna Kiss, and Bernadette Kálmán. 2024. “Vanishing White Matter Disease, a Rare Leukodystrophy with Mutation in the EIF2B5 Gene.” Clinical Neuroscience / Ideggyógyászati Szemle 77 (5/6): 207–11. doi:10.18071/isz.77.0207.