{"doi":"10.1002/9781118853771.ch15","title":"Lysosomal Storage Disorders","abstract":null,"journal":"Postgraduate Haematology","year":2015,"id":16124,"datarank":0.6076463857949921,"base_score":0.6931471805599453,"endowment":0.6931471805599453,"self_citation_contribution":0.10397207708399181,"citation_network_contribution":0.5036743087110003,"self_endowment_contribution":0.10397207708399181,"citer_contribution":0.5036743087110003,"corpus_percentile":null,"corpus_rank":null,"citation_count":1,"citer_count":1,"citers_with_citation_signal":1,"citers_with_endowment":1,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":120194,"name":"Derralynn A Hughes","orcid":null,"position":1,"is_corresponding":false},{"id":120193,"name":"Atul B Mehta","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"base_score":0.6931471805599453,"endowment":0.6931471805599453,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"21071399","pmcid":null,"openalex_id":"https://openalex.org/W2803960180","authors":[],"funders":[],"total_grants":0,"fwci":null,"citation_percentile":null,"influential_citations":14,"citation_trend":[],"oa_status":"closed","license":"http://doi.wiley.com/10.1002/tdm_license_1.1","oa_locations":[{"url":"http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2F9781118853771.ch15","host_type":"publisher"},{"url":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/9781118853771.ch15","host_type":"publisher"},{"url":"https://doi.org/10.1002/9781118853771.ch15","host_type":""}],"fields_of_study":["Lysosomal Storage Disorders Research","Trypanosoma species research and implications","Cellular transport and secretion","Medicine"],"mesh_terms":[],"keywords":["Substrate reduction therapy","Enzyme replacement therapy","Lysosomal storage disorders","Lysosomal storage disease","Lysosome","Disease","Glucocerebroside","Glucocerebrosidase","Fabry disease","Enzyme","Medicine","Transplantation","Cell","Chemistry","Biochemistry","Pathology","Internal medicine"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Good health and well-being"}],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-06-01T20:23:36.483723Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}