1. Tazir, Meriem, Nouioua, Sonia. 2024. Distal hereditary motor neuropathies. In Revue neurologique, 180, 1031-1036. doi:10.1016/j.neurol.2023.09.005. https://pubmed.ncbi.nlm.nih.gov/38702287/
2. Baviera-Muñoz, Raquel, Martínez-Rubio, Dolores, Sastre-Bataller, Isabel, Martínez-Torres, Irene, Espinós, Carmen. 2021. A 3.9-Mb Deletion on 2p11.2 Comprising the REEP1 Gene Causes Early-Onset Atypical Parkinsonism. In Neurology. Genetics, 7, e642. doi:10.1212/NXG.0000000000000642. https://pubmed.ncbi.nlm.nih.gov/34825060/
3. Guglielmi, Alessio. . A complete overview of REEP1: old and new insights on its role in hereditary spastic paraplegia and neurodegeneration. In Reviews in the neurosciences, 31, 351-362. doi:10.1515/revneuro-2019-0083. https://pubmed.ncbi.nlm.nih.gov/31913854/
4. Zhu, Peng-Peng, Hung, Hui-Fang, Batchenkova, Natalia, Hess, Harald F, Blackstone, Craig. . Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons. In Human molecular genetics, 31, 2779-2795. doi:10.1093/hmg/ddac072. https://pubmed.ncbi.nlm.nih.gov/35348668/