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