{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,25]],"date-time":"2025-11-25T14:23:46Z","timestamp":1764080626103,"version":"3.45.0"},"reference-count":17,"publisher":"BMJ","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[2001,11,1]]},"DOI":"10.1136\/jmg.38.11.e39","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T06:30:44Z","timestamp":1027751444000},"page":"e39-e39","source":"Crossref","is-referenced-by-count":6,"title":["Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cM"],"prefix":"10.1136","volume":"38","author":[{"given":"Shirley","family":"Rainier","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peter","family":"Hedera","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David","family":"Alvarado","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xinping","family":"Zhao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kleopas A","family":"Kleopa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Terry","family":"Heiman-Patterson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John K","family":"Fink","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2001,11,1]]},"reference":[{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.1","DOI":"10.1136\/jmg.38.1.65"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.2","DOI":"10.1007\/BF01667115"},{"key":"2025112506202077000_38.11.e39.3","doi-asserted-by":"crossref","first-page":"1507","DOI":"10.1212\/WNL.46.6.1507","article-title":"Hereditary spastic paraplegia: advances in genetic research.","volume":"46","author":"Fink","year":"1996","journal-title":"Neurology"},{"key":"2025112506202077000_38.11.e39.4","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1055\/s-2008-1040846","article-title":"Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.","volume":"19","author":"Fink","year":"1999","journal-title":"Semin Neurol"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.5","DOI":"10.1093\/hmg\/3.9.1569"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.6","DOI":"10.1038\/15472"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.7","DOI":"10.1093\/hmg\/3.10.1867"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.8","DOI":"10.1136\/jmg.35.2.89"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.9","DOI":"10.1086\/302776"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.10","DOI":"10.1086\/302258"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.11","DOI":"10.1086\/302783"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.12","DOI":"10.1086\/302555"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.13","DOI":"10.1086\/302241"},{"doi-asserted-by":"publisher","key":"2025112506202077000_38.11.e39.14","DOI":"10.1038\/ng1093-163"},{"key":"2025112506202077000_38.11.e39.15","doi-asserted-by":"crossref","first-page":"1216","DOI":"10.1101\/gr.8.11.1216","article-title":"Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.","volume":"8","author":"Paternotte","year":"1998","journal-title":"Genome Res"},{"key":"2025112506202077000_38.11.e39.16","first-page":"188","article-title":"Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.","volume":"56","author":"Fink","year":"1995","journal-title":"Am J Hum Genet"},{"key":"2025112506202077000_38.11.e39.17","first-page":"183","article-title":"Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.","volume":"56","author":"Gispert","year":"1995","journal-title":"Am J Hum Genet"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.38.11.e39","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,11,25]],"date-time":"2025-11-25T14:20:47Z","timestamp":1764080447000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.38.11.e39"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2001,11,1]]},"references-count":17,"journal-issue":{"issue":"11","published-online":{"date-parts":[[2001,11,1]]},"published-print":{"date-parts":[[2001,11,1]]}},"alternative-id":["10.1136\/jmg.38.11.e39"],"URL":"https:\/\/doi.org\/10.1136\/jmg.38.11.e39","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"type":"print","value":"0022-2593"},{"type":"electronic","value":"1468-6244"}],"subject":[],"published":{"date-parts":[[2001,11,1]]}}}