{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["15(2)"],"submitter":["Chen Y"],"funding":["National Natural Science Foundation of China","Science and Technology Department of Zhejiang Province"],"journal":["Journal of clinical neurology (Seoul, Korea)"],"pagination":["271-272"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6444155"],"repository":["biostudies-literature"],"pubmed_title":["A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia."],"pmcid":["PMC6444155"],"funding_grant_id":["31671301","81600850","81371266","81571089","81870895","2019C03017"],"pubmed_authors":["Zheng X","Xie F","Luo W","Cen Z","Chen Y","Chen S"],"additional_accession":[]},"is_claimable":false,"name":"A Novel Homozygous CAPN1 Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic Paraplegia.","description":null,"dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Apr","modification":"2025-04-26T18:17:38.567Z","creation":"2025-04-06T15:43:29.044Z"},"accession":"S-EPMC6444155","cross_references":{"pubmed":["30938113"],"doi":["10.3988/jcn.2019.15.2.271"]}}