1. Votsi, Christina, Ververis, Antonis, Nicolaou, Paschalis, Christodoulou, Kyproula, Zamba-Papanicolaou, Eleni. 2022. A Novel SPG7 Gene Pathogenic Variant in a Cypriot Family With Autosomal Recessive Spastic Ataxia. In Frontiers in genetics, 12, 812640. doi:10.3389/fgene.2021.812640. https://pubmed.ncbi.nlm.nih.gov/35096021/
2. Eriksen, Kathrine O, Wigers, Andreas Reidar, Wedding, Iselin Marie, Søberg, Kristoffer, Jørstad, Øystein Kalsnes. 2022. A novel homozygous variant in the SPG7 gene presenting with childhood optic nerve atrophy. In American journal of ophthalmology case reports, 26, 101400. doi:10.1016/j.ajoc.2022.101400. https://pubmed.ncbi.nlm.nih.gov/35243150/
3. Méreaux, Jean-Loup, Banneau, Guillaume, Papin, Mélanie, Leguern, Eric, Stevanin, Giovanni. . Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia. In Brain : a journal of neurology, 145, 1029-1037. doi:10.1093/brain/awab386. https://pubmed.ncbi.nlm.nih.gov/34983064/
4. Zhang, Yaodan, Miao, Yuyang, Tan, Jin, Lei, Ping, Zhang, Qiang. 2023. Identification of mitochondrial related signature associated with immune microenvironment in Alzheimer's disease. In Journal of translational medicine, 21, 458. doi:10.1186/s12967-023-04254-9. https://pubmed.ncbi.nlm.nih.gov/37434203/
5. Fink, John K. 2013. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. In Acta neuropathologica, 126, 307-28. doi:10.1007/s00401-013-1115-8. https://pubmed.ncbi.nlm.nih.gov/23897027/
6. Chinnery, P F, Schon, E A. . Mitochondria. In Journal of neurology, neurosurgery, and psychiatry, 74, 1188-99. doi:. https://pubmed.ncbi.nlm.nih.gov/12933917/
7. Settasatian, C, Whitmore, S A, Crawford, J, Sutherland, G R, Callen, D F. . Genomic structure and expression analysis of the spastic paraplegia gene, SPG7. In Human genetics, 105, 139-44. doi:. https://pubmed.ncbi.nlm.nih.gov/10480368/
8. Seo, Yuri, Lim, Hyun Taek, Lee, Byung Joo, Han, Jinu. 2022. Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia. In American journal of medical genetics. Part A, 191, 582-585. doi:10.1002/ajmg.a.63037. https://pubmed.ncbi.nlm.nih.gov/36367250/