{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T04:06:27Z","timestamp":1790136387407,"version":"4.0.1"},"reference-count":21,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100003478","name":"Ministry of Health, Labour and Welfare","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003478","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001691","name":"Japan Society for the Promotion of Science","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100001691","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100009619","name":"Japan Agency for Medical Research and Development","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100009619","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jns-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2020,5]]},"DOI":"10.1016\/j.jns.2020.116795","type":"journal-article","created":{"date-parts":[[2020,3,24]],"date-time":"2020-03-24T19:45:10Z","timestamp":1585079110000},"page":"116795","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":8,"special_numbering":"C","title":["Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients"],"prefix":"10.1016","volume":"412","author":[{"given":"Maki","family":"Nakaza","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuri","family":"Kitamura","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mitsuru","family":"Furuta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tomoya","family":"Kubota","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ryogen","family":"Sasaki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5513-5012","authenticated-orcid":false,"given":"Masanori P.","family":"Takahashi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jns.2020.116795_bb0005","doi-asserted-by":"crossref","first-page":"522","DOI":"10.1002\/mus.26009","article-title":"Review of the diagnosis and treatment of periodic paralysis","volume":"57","author":"Statland","year":"2018","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.jns.2020.116795_bb0010","doi-asserted-by":"crossref","first-page":"1544","DOI":"10.1212\/01.wnl.0000342387.65477.46","article-title":"Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis","volume":"72","author":"Matthews","year":"2009","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2020.116795_bb0015","doi-asserted-by":"crossref","first-page":"761","DOI":"10.1002\/j.2040-4603.2015.tb00630.x","article-title":"Channelopathies of skeletal muscle excitability","volume":"5","author":"Cannon","year":"2015","journal-title":"Compr. Physiol."},{"key":"10.1016\/j.jns.2020.116795_bb0020","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1038\/nature05598","article-title":"Gating pore current in an inherited ion channelopathy","volume":"446","author":"Sokolov","year":"2007","journal-title":"Nature"},{"key":"10.1016\/j.jns.2020.116795_bb0025","doi-asserted-by":"crossref","first-page":"511","DOI":"10.1016\/S0092-8674(01)00342-7","article-title":"Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen\u2019s syndrome","volume":"105","author":"Plaster","year":"2001","journal-title":"Cell"},{"key":"10.1016\/j.jns.2020.116795_bb0030","doi-asserted-by":"crossref","first-page":"985","DOI":"10.1681\/ASN.2012010046","article-title":"Mechanism of thyrotoxic periodic paralysis","volume":"23","author":"Lin","year":"2012","journal-title":"J. Am. Soc. Nephrol."},{"key":"10.1016\/j.jns.2020.116795_bb0035","doi-asserted-by":"crossref","first-page":"657","DOI":"10.1038\/nrendo.2011.58","article-title":"Novel etiopathophysiological aspects of thyrotoxic periodic paralysis","volume":"7","author":"Maciel","year":"2011","journal-title":"Nat. Rev. Endocrinol."},{"key":"10.1016\/j.jns.2020.116795_bb0040","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1016\/j.cell.2009.12.024","article-title":"Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis","volume":"140","author":"Ryan","year":"2010","journal-title":"Cell"},{"key":"10.1016\/j.jns.2020.116795_bb0045","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1038\/jhg.2012.20","article-title":"A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis","volume":"57","author":"Jongjaroenprasert","year":"2012","journal-title":"J. Hum. Genet."},{"key":"10.1016\/j.jns.2020.116795_bb0050","doi-asserted-by":"crossref","first-page":"1026","DOI":"10.1038\/ng.2367","article-title":"Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3","volume":"44","author":"Cheung","year":"2012","journal-title":"Nat. Genet."},{"key":"10.1016\/j.jns.2020.116795_bb0055","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/j.cca.2012.08.004","article-title":"Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis","volume":"414","author":"Chu","year":"2012","journal-title":"Clin. Chim. Acta"},{"key":"10.1016\/j.jns.2020.116795_bb0060","doi-asserted-by":"crossref","first-page":"38","DOI":"10.1186\/s12883-015-0290-8","article-title":"The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis","volume":"15","author":"Li","year":"2015","journal-title":"BMC Neurol."},{"key":"10.1016\/j.jns.2020.116795_bb0065","doi-asserted-by":"crossref","first-page":"1190","DOI":"10.1212\/WNL.0000000000002524","article-title":"Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis","volume":"86","author":"Song","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2020.116795_bb0070","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1002\/ana.22238","article-title":"Refined exercise testing can aid dna-based diagnosis in muscle channelopathies","volume":"69","author":"Tan","year":"2011","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.jns.2020.116795_bb0075","doi-asserted-by":"crossref","first-page":"784","DOI":"10.1002\/mus.20865","article-title":"Muscle membrane excitability after exercise in thyrotoxic periodic paralysis and thyrotoxicosis without periodic paralysis","volume":"36","author":"Arimura","year":"2007","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.jns.2020.116795_bb0080","author":"1000 Genomes"},{"key":"10.1016\/j.jns.2020.116795_bb0085","author":"Japanese Multi Omics Reference Panel"},{"key":"10.1016\/j.jns.2020.116795_bb0090","author":"Genome aggregation database"},{"key":"10.1016\/j.jns.2020.116795_bb0095","author":"The Human Protein Atlas"},{"key":"10.1016\/j.jns.2020.116795_bb0100","doi-asserted-by":"crossref","first-page":"809","DOI":"10.1210\/js.2017-00015","article-title":"Novel lincRNA susceptibility gene and its role in Etiopathogenesis of Thyrotoxic periodic paralysis","volume":"1","author":"Melo","year":"2017","journal-title":"J. Endocr. Soc."},{"key":"10.1016\/j.jns.2020.116795_bb0105","author":"Genome Reference Consortium"}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X20301313?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X20301313?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,20]],"date-time":"2025-09-20T15:52:20Z","timestamp":1758383540000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X20301313"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,5]]},"references-count":21,"alternative-id":["S0022510X20301313"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2020.116795","relation":{},"ISSN":["0022-510X"],"issn-type":[{"value":"0022-510X","type":"print"}],"subject":[],"published":{"date-parts":[[2020,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients","name":"articletitle","label":"Article Title"},{"value":"Journal of the Neurological Sciences","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jns.2020.116795","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"116795"}}