{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,2]],"date-time":"2025-10-02T00:48:28Z","timestamp":1759366108774,"version":"build-2065373602"},"reference-count":6,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,6,1]],"date-time":"2020-06-01T00:00:00Z","timestamp":1590969600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,1,20]],"date-time":"2020-01-20T00:00:00Z","timestamp":1579478400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["clinicalkey.es","elsevier.es","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neurolog\u00eda"],"published-print":{"date-parts":[[2020,6]]},"DOI":"10.1016\/j.nrl.2018.01.014","type":"journal-article","created":{"date-parts":[[2018,3,8]],"date-time":"2018-03-08T09:46:04Z","timestamp":1520502364000},"page":"340-341","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":0,"title":["Nueva variante patog\u00e9nica en el gen SPAST en una familia espa\u00f1ola afecta de paraplej\u00eda esp\u00e1stica hereditaria"],"prefix":"10.1016","volume":"35","author":[{"given":"B.","family":"Bertran Recasens","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Figueras Aguirre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Aznar-Lain","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.A.","family":"Rubio","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.nrl.2018.01.014_bib0035","doi-asserted-by":"crossref","first-page":"506","DOI":"10.1126\/science.1247363","article-title":"Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders","volume":"343","author":"Novarino","year":"2014","journal-title":"Science"},{"key":"10.1016\/j.nrl.2018.01.014_bib0040","doi-asserted-by":"crossref","first-page":"e122","DOI":"10.1212\/NXG.0000000000000122","article-title":"Clinical and genetic study of hereditary spastic paraplegia in Canada","volume":"3","author":"Chrestian","year":"2016","journal-title":"Neurol Genet"},{"key":"10.1016\/j.nrl.2018.01.014_bib0045","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1016\/S0962-8924(97)01212-9","article-title":"The AAA team: Related ATPases with diverse functions","volume":"8","author":"Patel","year":"1998","journal-title":"Trends Cell Biol"},{"key":"10.1016\/j.nrl.2018.01.014_bib0050","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1136\/jmg.40.2.81","article-title":"Science in motion: Common molecular pathological themes emerge in the hereditary spastic paraplegias","volume":"40","author":"Reid","year":"2003","journal-title":"J Med Genet"},{"key":"10.1016\/j.nrl.2018.01.014_bib0055","first-page":"e75","article-title":"Child neurology: Hereditary spastic paraplegia in children","volume":"75","author":"de Biot","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.nrl.2018.01.014_bib0060","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1038\/gim.2015.30","article-title":"Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology","volume":"17","author":"Richards","year":"2015","journal-title":"Genet Med"}],"container-title":["Neurolog\u00eda"],"original-title":[],"language":"es","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0213485318300367?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0213485318300367?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,1]],"date-time":"2025-10-01T13:11:45Z","timestamp":1759324305000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0213485318300367"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,6]]},"references-count":6,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2020,6]]}},"alternative-id":["S0213485318300367"],"URL":"https:\/\/doi.org\/10.1016\/j.nrl.2018.01.014","relation":{},"ISSN":["0213-4853"],"issn-type":[{"type":"print","value":"0213-4853"}],"subject":[],"published":{"date-parts":[[2020,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Nueva variante patog\u00e9nica en el gen SPAST en una familia espa\u00f1ola afecta de paraplej\u00eda esp\u00e1stica hereditaria","name":"articletitle","label":"Article Title"},{"value":"Neurolog\u00eda","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nrl.2018.01.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Sociedad Espa\u00f1ola de Neurolog\u00eda. Published by Elsevier Espa\u00f1a, S.L.U.","name":"copyright","label":"Copyright"}]}}