{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T06:39:31Z","timestamp":1649140771875},"reference-count":4,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2018,9,1]],"date-time":"2018-09-01T00:00:00Z","timestamp":1535760000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","ejpn-journal.com","clinicalkey.es","clinicalkey.fr","clinicalkey.com.au","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Paediatric Neurology"],"published-print":{"date-parts":[[2018,9]]},"DOI":"10.1016\/j.ejpn.2018.04.011","type":"journal-article","created":{"date-parts":[[2018,4,30]],"date-time":"2018-04-30T09:56:10Z","timestamp":1525082170000},"page":"892-893","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"title":["Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)"],"prefix":"10.1016","volume":"22","author":[{"given":"Pasquale","family":"Striano","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Giulia","family":"Iapadre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maria Stella","family":"Vari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alberto","family":"Verrotti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"5","key":"10.1016\/j.ejpn.2018.04.011_bib1","doi-asserted-by":"crossref","first-page":"889","DOI":"10.1016\/j.ejpn.2018.04.012","article-title":"CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder","volume":"22","author":"Finsterer","year":"2018","journal-title":"Eur J Paediatr Neurol"},{"issue":"3","key":"10.1016\/j.ejpn.2018.04.011_bib2","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1016\/j.ejpn.2017.12.020","article-title":"A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype","volume":"22","author":"Iapadre","year":"2018","journal-title":"Eur J Paediatr Neurol"},{"key":"10.1016\/j.ejpn.2018.04.011_bib3","doi-asserted-by":"crossref","first-page":"380","DOI":"10.1111\/jns.12145","article-title":"Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations","volume":"20","author":"Piscosquito","year":"2015","journal-title":"J Peripher Nerv Syst"},{"key":"10.1016\/j.ejpn.2018.04.011_bib4","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1212\/WNL.0b013e3182242d4d","article-title":"Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations","volume":"77","author":"Polke","year":"2011","journal-title":"Neurology"}],"container-title":["European Journal of Paediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379818301880?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379818301880?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,11]],"date-time":"2018-09-11T03:41:34Z","timestamp":1536637294000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1090379818301880"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,9]]},"references-count":4,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2018,9]]}},"alternative-id":["S1090379818301880"],"URL":"https:\/\/doi.org\/10.1016\/j.ejpn.2018.04.011","relation":{},"ISSN":["1090-3798"],"issn-type":[{"value":"1090-3798","type":"print"}],"subject":[],"published":{"date-parts":[[2018,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)","name":"articletitle","label":"Article Title"},{"value":"European Journal of Paediatric Neurology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejpn.2018.04.011","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"https:\/\/doi.org\/10.1016\/j.ejpn.2018.04.012","name":"associatedlink","label":"CrossRef DOI link to the associated document"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}