{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T19:02:50Z","timestamp":1793473370326,"version":"4.5.0"},"reference-count":53,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,11,1]],"date-time":"2019-11-01T00:00:00Z","timestamp":1572566400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/100009647","name":"Ministry of Health","doi-asserted-by":"publisher","award":["NET-2013-02356160"],"award-info":[{"award-number":["NET-2013-02356160"]}],"id":[{"id":"10.13039\/100009647","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","prd-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Parkinsonism &amp; Related Disorders"],"published-print":{"date-parts":[[2019,11]]},"DOI":"10.1016\/j.parkreldis.2019.09.015","type":"journal-article","created":{"date-parts":[[2019,9,28]],"date-time":"2019-09-28T13:55:17Z","timestamp":1569678917000},"page":"8-16","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":34,"special_numbering":"C","title":["Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review"],"prefix":"10.1016","volume":"68","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4717-699X","authenticated-orcid":false,"given":"Serena","family":"Galosi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Emanuele","family":"Barca","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rosalba","family":"Carrozzo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2517-6278","authenticated-orcid":false,"given":"Tommaso","family":"Schirinzi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catarina Maria","family":"Quinzii","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria","family":"Lieto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gessica","family":"Vasco","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ginevra","family":"Zanni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michela","family":"Di Nottia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniele","family":"Galatolo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alessandro","family":"Filla","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Enrico","family":"Bertini","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Filippo Maria","family":"Santorelli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vincenzo","family":"Leuzzi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard","family":"Haas","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michio","family":"Hirano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jennifer","family":"Friedman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.parkreldis.2019.09.015_bib1","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1007\/s10545-014-9749-9","article-title":"Genetic bases and clinical manifestations of coenzyme Q 10 (CoQ 10) deficiency","volume":"38","author":"Desbats","year":"2015","journal-title":"J. Inherit. Metab. Dis."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib2","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1016\/j.biochi.2013.12.006","article-title":"The molecular genetics of coenzyme Q biosynthesis in health and disease","volume":"100","author":"Laredj","year":"2014","journal-title":"Biochimie"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib3","doi-asserted-by":"crossref","first-page":"978","DOI":"10.1001\/archneurol.2012.206","article-title":"Heterogeneity of coenzyme Q10 deficiency: patient study and literature review","volume":"69","author":"Emmanuele","year":"2012","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib4","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/humu.23345","article-title":"A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C\u2010methyltransferase deficiency","volume":"39","author":"Malicdan","year":"2018","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib5","doi-asserted-by":"crossref","first-page":"779","DOI":"10.1136\/jmedgenet-2015-102986","article-title":"Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2, 4\u2013dihydroxybensoic acid","volume":"52","author":"Freyer","year":"2015","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib6","doi-asserted-by":"crossref","first-page":"2329","DOI":"10.1111\/jcmm.13154","article-title":"Pathogenicity of two COQ7 mutations and responses to 2, 4\u2010dihydroxybenzoate bypass treatment","volume":"21","author":"Wang","year":"2017","journal-title":"J. Cell Mol. Med."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib7","doi-asserted-by":"crossref","first-page":"3733","DOI":"10.1096\/fj.09-152728","article-title":"Reactive oxygen species, oxidative stress, and cell death correlate with level of CoQ10 deficiency","volume":"24","author":"Quinzii","year":"2010","journal-title":"FASEB J."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib8","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1159\/000362942","article-title":"An overview of current mouse models recapitulating coenzyme q10 deficiency syndrome","volume":"5","author":"Licitra","year":"2014","journal-title":"Mol Syndromol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib9","doi-asserted-by":"crossref","first-page":"78","DOI":"10.15252\/emmm.201606345","article-title":"CoQ deficiency causes disruption of mitochondrial sulfide oxidation, a new pathomechanism associated to this syndrome","volume":"9","author":"Luna-S\u00e1nchez","year":"2017","journal-title":"EMBO Mol. Med."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib10","doi-asserted-by":"crossref","first-page":"96","DOI":"10.15252\/emmm.201606356","article-title":"Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway","volume":"9","author":"Ziosi","year":"2017","journal-title":"EMBO Mol. Med."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib11","doi-asserted-by":"crossref","first-page":"1912","DOI":"10.1126\/science.1075762","article-title":"The protein kinase complement of the human genome","volume":"298","author":"Manning","year":"2002","journal-title":"Science"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib12","doi-asserted-by":"crossref","first-page":"608","DOI":"10.1016\/j.molcel.2016.06.030","article-title":"Cerebellar ataxia and coenzyme q deficiency through loss of unorthodox kinase activity","volume":"63","author":"Stefely","year":"2016","journal-title":"Mol. Cell"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib13","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.molcel.2014.11.002","article-title":"Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis","volume":"57","author":"Stefely","year":"2015","journal-title":"Mol. Cell"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib14","doi-asserted-by":"crossref","first-page":"154","DOI":"10.1016\/j.chembiol.2017.11.001","article-title":"Conserved lipid and small-molecule modulation of COQ8 reveals regulation of the ancient kinase-like UbiB family","volume":"25","author":"Reidenbach","year":"2018","journal-title":"Cell Chem. Biol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib15","article-title":"AarF domain containing kinase 3 (ADCK3) mutant cells display signs of oxidative stress, defects in mitochondrial homeostasis and lysosomal accumulation","volume":"11","author":"Cullen","year":"2016","journal-title":"PLoS One"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib16","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1016\/j.ajhg.2007.12.022","article-title":"CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures","volume":"82","author":"Mollet","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib17","doi-asserted-by":"crossref","first-page":"661","DOI":"10.1016\/j.ajhg.2007.12.024","article-title":"ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency","volume":"82","author":"Lagier-Tourenne","year":"2008","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib18","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1016\/j.mito.2010.05.008","article-title":"Nonsense mutations in CABC1\/ADCK3 cause progressive cerebellar ataxia and atrophy","volume":"10","author":"Gerards","year":"2010","journal-title":"Mitochondrion"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib19","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1136\/jnnp-2011-301258","article-title":"Adult-onset cerebellar ataxia due to mutations in CABC1\/ADCK3","volume":"83","author":"Horvath","year":"2012","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib20","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1016\/j.ejpn.2011.07.016","article-title":"The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children","volume":"16","author":"Terracciano","year":"2012","journal-title":"Eur. J. Paediatr. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib21","doi-asserted-by":"crossref","first-page":"493","DOI":"10.1136\/jnnp-2013-306483","article-title":"Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterization","volume":"84","author":"Liu","year":"2014","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib22","first-page":"103","article-title":"Heterozygous mutations in the ADCK3 gene in siblings with cerebellar atrophy and extreme phenotypic variability","volume":"12","author":"Blumkin","year":"2013","journal-title":"JIMD Rep"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib23","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1186\/1750-1172-8-173","article-title":"Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression","volume":"8","author":"Mignot","year":"2013","journal-title":"Orphanet J. Rare Dis."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib24","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1111\/cge.12742","article-title":"Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3","volume":"90","author":"Barca","year":"2016","journal-title":"Clin. Genet."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib25","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1016\/j.parkreldis.2016.10.010","article-title":"A novel CABC1\/ADCK3 mutation in adult-onset cerebellar ataxia","volume":"33","author":"Malgireddy","year":"2016","journal-title":"Park. Relat. Disord."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib26","doi-asserted-by":"crossref","first-page":"1188","DOI":"10.1111\/ene.13003","article-title":"ADCK3 mutations with epilepsy, stroke\u2010like episodes and ataxia: a POLG mimic?","volume":"23","author":"Hikmat","year":"2016","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib27","first-page":"31","article-title":"Compound heterozygous inheritance of mutations in coenzyme Q8A results in autosomal recessive cerebellar ataxia and coenzyme Q10 deficiency in a female sib-pair","volume":"42","author":"Jacobsen","year":"2018","journal-title":"JIMD Rep"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib28","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1002\/mdc3.12667","article-title":"ADCK3\u2010related coenzyme Q10 deficiency: a potentially treatable genetic disease","volume":"5","author":"Chang","year":"2018","journal-title":"Mov. Disord. Clin. Pract."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib29","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1038\/s41436-018-0007-7","article-title":"Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes","volume":"21","author":"Sun","year":"2019","journal-title":"Genet. Med."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib30","doi-asserted-by":"crossref","first-page":"743","DOI":"10.1016\/S2213-8587(16)30320-5","article-title":"Key European guidelines for the diagnosis and management of patients with phenylketonuria","volume":"5","author":"van Spronsen","year":"2017","journal-title":"Lancet Diabetes Endocrinol"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib31","doi-asserted-by":"crossref","first-page":"D840","DOI":"10.1093\/nar\/gkw971","article-title":"The ExAC browser: displaying reference data information from over 60 000 exomes","volume":"45","author":"Karczewski","year":"2017","journal-title":"Nucleic Acids Res."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib32","doi-asserted-by":"crossref","first-page":"D862","DOI":"10.1093\/nar\/gkv1222","article-title":"ClinVar: public archive of interpretations of clinically relevant variants","volume":"44","author":"Landrum","year":"2015","journal-title":"Nucleic Acids Res."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib33","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1002\/ddrr.108","article-title":"Coenzyme Q and mitochondrial disease","volume":"16","author":"Quinzii","year":"2010","journal-title":"Dev. Disabil. Res. Rev."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib34","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1016\/S0140-6736(14)60041-6","article-title":"Imaging insights into basal ganglia function, Parkinson's disease, and dystonia","volume":"384","author":"Stoessl","year":"2014","journal-title":"Lancet"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib35","article-title":"The anatomical basis for dystonia: the motor network model","volume":"7","author":"Jinnah","year":"2017","journal-title":"Tremor. Other. Hyperkinet. Mov."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib36","doi-asserted-by":"crossref","DOI":"10.1186\/s40673-017-0064-8","article-title":"Cerebellum: an explanation for dystonia?","volume":"4","author":"Bologna","year":"2017","journal-title":"Cerebellum. Ataxias"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib37","doi-asserted-by":"crossref","first-page":"577","DOI":"10.1007\/s12311-016-0825-6","article-title":"Current opinions and areas of consensus on the role of the cerebellum in dystonia","volume":"16","author":"Shakkottai","year":"2017","journal-title":"Cerebellum"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib38","doi-asserted-by":"crossref","first-page":"498","DOI":"10.1097\/WCO.0000000000000580","article-title":"Dystonia as a network disorder: a concept in evolution","volume":"31","author":"Schirinzi","year":"2018","journal-title":"Curr. Opin. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib39","doi-asserted-by":"crossref","first-page":"1767","DOI":"10.1038\/nn.3868","article-title":"Short latency cerebellar modulation of the basal ganglia","volume":"17","author":"Chen","year":"2014","journal-title":"Nat. Neurosci."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib40","doi-asserted-by":"crossref","first-page":"90","DOI":"10.1016\/j.nicl.2017.10.011","article-title":"Loss of inhibition in sensorimotor networks in focal hand dystonia","volume":"17","author":"Gallea","year":"2018","journal-title":"Neuroimage. Clin"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib41","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/j.nicl.2018.01.015","article-title":"Dynamic causal modeling revealed dysfunctional effective connectivity in both, the cortico-basal-ganglia and the cerebello-cortical motor network in writers' cramp","volume":"18","author":"Rothkirch","year":"2018","journal-title":"Neuroimage. Clin."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib42","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1002\/mds.10308","article-title":"Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?","volume":"18","author":"Kuoppam\u00e4ki","year":"2003","journal-title":"Mov. Disord."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib43","doi-asserted-by":"crossref","first-page":"1769","DOI":"10.1212\/01.wnl.0000244484.60489.50","article-title":"Predominant dystonia with marked cerebellar atrophy A rare phenotype in familial dystonia","volume":"67","author":"Le Ber","year":"2006","journal-title":"Neurology"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib44","doi-asserted-by":"crossref","first-page":"774","DOI":"10.1136\/jnnp.2006.105841","article-title":"The syndrome of (predominantly cervical) dystonia and cerebellar ataxia: new cases indicate a distinct but heterogeneous entity","volume":"78","author":"van de Warrenburg","year":"2007","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib45","doi-asserted-by":"crossref","first-page":"e1","DOI":"10.1212\/WNL.0000000000002232","article-title":"Pearls & Oy-sters: spinocerebellar ataxia type 3 presenting with cervical dystonia without ataxia","volume":"86","author":"Muglan","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib46","doi-asserted-by":"crossref","first-page":"684","DOI":"10.1080\/00207454.2017.1408621","article-title":"Spinocerebellar ataxia type 3 presenting with writer's cramp without ataxia","volume":"128","author":"M\u00e9ndez-Guerrero","year":"2017","journal-title":"Int. J. Neurosci."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib47","doi-asserted-by":"crossref","first-page":"1444","DOI":"10.1136\/jnnp.74.10.1444","article-title":"Task specific focal dystonia: a presentation of spinocerebellar ataxia type 6","volume":"74","author":"Muzaimi","year":"2003","journal-title":"J. Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib48","doi-asserted-by":"crossref","unstructured":"D.A. Olszewska, R. Walsh, T. Lynch, SCA 6 with writer's cramp: the phenotype expanded, Mov Disord Clin Pract. 3 (1) 83-86.","DOI":"10.1002\/mdc3.12222"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib49","doi-asserted-by":"crossref","first-page":"589","DOI":"10.1016\/S0035-3787(07)90465-8","article-title":"Writer's cramp secondary to spinocerebellar ataxia type 7","volume":"163","author":"Gaillard","year":"2007","journal-title":"Rev. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib50","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1002\/mdc3.12109","article-title":"Writer's cramp as the first symptom of spinocerebellar ataxia 14","volume":"2","author":"Erro","year":"2015","journal-title":"Mov Disord Clin Pract"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib51","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1007\/s12311-013-0522-7","article-title":"Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14","volume":"13","author":"Ganos","year":"2014","journal-title":"Cerebellum"},{"key":"10.1016\/j.parkreldis.2019.09.015_bib52","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1007\/s00415-013-7177-7","article-title":"Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation","volume":"261","author":"Doss","year":"2014","journal-title":"J. Neurol."},{"key":"10.1016\/j.parkreldis.2019.09.015_bib53","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1002\/mds.27174","article-title":"Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum","volume":"33","author":"Schreglmann","year":"2018","journal-title":"Mov. Disord."}],"container-title":["Parkinsonism &amp; Related Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S135380201930392X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S135380201930392X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T00:16:46Z","timestamp":1761178606000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S135380201930392X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,11]]},"references-count":53,"alternative-id":["S135380201930392X"],"URL":"https:\/\/doi.org\/10.1016\/j.parkreldis.2019.09.015","relation":{},"ISSN":["1353-8020"],"issn-type":[{"value":"1353-8020","type":"print"}],"subject":[],"published":{"date-parts":[[2019,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Dystonia-Ataxia with early handwriting deterioration in COQ8A mutation carriers: A case series and literature review","name":"articletitle","label":"Article Title"},{"value":"Parkinsonism & Related Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.parkreldis.2019.09.015","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}]}}