1. Filareto, Ilaria, Cinelli, Giulia, Scalabrini, Ilaria, Todeschini, Alessandra, Iughetti, Lorenzo. 2022. EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report. In Italian journal of pediatrics, 48, 128. doi:10.1186/s13052-022-01325-3. https://pubmed.ncbi.nlm.nih.gov/35897042/
2. Sambati, Luisa, Agati, Raffaele, Bacci, Antonella, Bianchi, Silvia, Capellari, Sabina. 2012. Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course. In Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 34, 1235-8. doi:10.1007/s10072-012-1129-3. https://pubmed.ncbi.nlm.nih.gov/22729508/
3. Wei, Cuibai, Qin, Qi, Chen, Fei, Lyu, Jihui, Jia, Jianping. 2019. Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia. In BMC neurology, 19, 203. doi:10.1186/s12883-019-1429-9. https://pubmed.ncbi.nlm.nih.gov/31438897/
4. Bian, Rutao, Li, Dongyu, Xu, Xuegong, Zhang, Li. . The impact of immunity on the risk of coronary artery disease: insights from a multiomics study. In Postgraduate medical journal, 101, 50-59. doi:10.1093/postmj/qgae105. https://pubmed.ncbi.nlm.nih.gov/39180487/
5. Hasbani, Natalie R, Westerman, Kenneth E, Kwak, Soo Heon, Manning, Alisa K, de Vries, Paul S. 2023. Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. In Circulation. Genomic and precision medicine, 16, e004176. doi:10.1161/CIRCGEN.123.004176. https://pubmed.ncbi.nlm.nih.gov/38014529/
6. Illés, Anett, Pikó, Henriett, Árvai, Kristóf, Lakatos, Péter, Beke, Artúr. 2024. Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing. In BMC medical genomics, 17, 98. doi:10.1186/s12920-024-01873-z. https://pubmed.ncbi.nlm.nih.gov/38649916/
7. Pronk, Jan C, van Kollenburg, Barbara, Scheper, Gert C, van der Knaap, Marjo S. . Vanishing white matter disease: a review with focus on its genetics. In Mental retardation and developmental disabilities research reviews, 12, 123-8. doi:. https://pubmed.ncbi.nlm.nih.gov/16807905/