{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,6]],"date-time":"2025-10-06T06:01:45Z","timestamp":1759730505879,"version":"3.44.0"},"reference-count":39,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2008,6,1]],"date-time":"2008-06-01T00:00:00Z","timestamp":1212278400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","internationaljournalofcardiology.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["International Journal of Cardiology"],"published-print":{"date-parts":[[2008,6]]},"DOI":"10.1016\/j.ijcard.2007.02.049","type":"journal-article","created":{"date-parts":[[2007,5,8]],"date-time":"2007-05-08T09:33:38Z","timestamp":1178616818000},"page":"439-442","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":19,"title":["The search of \u2018novel\u2019 mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor"],"prefix":"10.1016","volume":"126","author":[{"given":"Hans-J\u00fcrgen","family":"Bandelt","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yong-Gang","family":"Yao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antonio","family":"Salas","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ijcard.2007.02.049_bib1","doi-asserted-by":"crossref","first-page":"e296","DOI":"10.1371\/journal.pmed.0020296","article-title":"A critical reassessment of the role of mitochondria in tumorigenesis","volume":"2","author":"Salas","year":"2005","journal-title":"PLoS Med"},{"key":"10.1016\/j.ijcard.2007.02.049_bib2","doi-asserted-by":"crossref","first-page":"1073","DOI":"10.1007\/s10038-006-0066-5","article-title":"What is a \u2018novel\u2019 mtDNA mutation \u2014 and does \u2018novelty\u2019 really matter?","volume":"51","author":"Bandelt","year":"2006","journal-title":"J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib3","doi-asserted-by":"crossref","first-page":"432","DOI":"10.1016\/j.ijcard.2005.07.065","article-title":"Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy","volume":"109","author":"Prasad","year":"2006","journal-title":"Int J Cardiol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib4","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1186\/1471-2164-7-151","article-title":"In situ origin of deep rooting lineages of mitochondrial macrohaplogroup M in India","volume":"7","author":"Thangaraj","year":"2006","journal-title":"BMC Genomics"},{"key":"10.1016\/j.ijcard.2007.02.049_bib5","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1016\/j.ijcard.2006.07.229","article-title":"Novel mithochonrial DNA mutauions implicated in Noonan syndrome","volume":"120","author":"Dhandapany","year":"2007","journal-title":"Int J Cardiol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib6","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1002\/ajmg.b.30302","article-title":"Clinical and genetic uniqueness in an individual with MELAS","volume":"141B","author":"Vanniarajan","year":"2006","journal-title":"Am J Med Genet Part B"},{"key":"10.1016\/j.ijcard.2007.02.049_bib7","doi-asserted-by":"crossref","first-page":"683","DOI":"10.1093\/molbev\/msj078","article-title":"The dazzling array of basal branches in the mtDNA macrohaplogroup M from India as inferred from complete genomes","volume":"23","author":"Sun","year":"2006","journal-title":"Mol Biol Evol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib8","doi-asserted-by":"crossref","first-page":"966","DOI":"10.1086\/425871","article-title":"Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia","volume":"75","author":"Palanichamy","year":"2004","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib9","doi-asserted-by":"crossref","first-page":"1152","DOI":"10.1086\/339933","article-title":"Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences from the major African, Asian, and European haplogroups","volume":"70","author":"Herrnstadt","year":"2002","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib10","unstructured":"Parson TJ (unpublished). GenBank accession numbers: DQ304897, DQ304898, DQ304899, DQ304899, DQ304900, DQ304903, and DQ304987."},{"key":"10.1016\/j.ijcard.2007.02.049_bib11","doi-asserted-by":"crossref","first-page":"549","DOI":"10.1086\/367849","article-title":"Accumulation of mitochondrial DNA mutations in human immunodeficiency virus-infected patients treated with nucleoside-analogue reverse-transcriptase inhibitors","volume":"72","author":"Martin","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib12","unstructured":"Trejaut JA, Loo J-H, Lin M (unpublished). GenBank accession number: EF093547."},{"key":"10.1016\/j.ijcard.2007.02.049_bib13","doi-asserted-by":"crossref","first-page":"1832","DOI":"10.1101\/gr.2286304","article-title":"Mitochondrial genome variation in eastern Asia and the peopling of Japan","volume":"14","author":"Tanaka","year":"2004","journal-title":"Genome Res"},{"key":"10.1016\/j.ijcard.2007.02.049_bib14","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1534\/genetics.105.043901","article-title":"The role of selection in the evolution of human mitochondrial genomes","volume":"172","author":"Kivisild","year":"2006","journal-title":"Genetics"},{"key":"10.1016\/j.ijcard.2007.02.049_bib15","doi-asserted-by":"crossref","first-page":"1600","DOI":"10.1101\/gr.686603","article-title":"Mitochondrial genome variation and evolutionary history of Australian and New Guinean aborigines","volume":"13","author":"Ingman","year":"2003","journal-title":"Genome Res"},{"key":"10.1016\/j.ijcard.2007.02.049_bib16","doi-asserted-by":"crossref","first-page":"506","DOI":"10.1016\/S0960-8966(01)00329-7","article-title":"Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene","volume":"12","author":"Yamasoba","year":"2002","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.ijcard.2007.02.049_bib17","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1093\/molbev\/msm004","article-title":"No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males","volume":"24","author":"Pereira","year":"2007","journal-title":"Mol Biol Evol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib18","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1080\/00016480310015740","article-title":"A novel mitochondrial mutation, 1556C>T, in a Japanese patient with streptomycin-induced tinnitus","volume":"124","author":"Tanimoto","year":"2004","journal-title":"Acta Otolaryngol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib19","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1517\/14622416.6.1.27","article-title":"Genetic factors in aminoglycoside toxicity","volume":"6","author":"Fischel-Ghodsian","year":"2005","journal-title":"Pharmacogenomics"},{"key":"10.1016\/j.ijcard.2007.02.049_bib20","doi-asserted-by":"crossref","first-page":"708","DOI":"10.1038\/35047064","article-title":"Mitochondrial genome variation and the origin of modern humans","volume":"408","author":"Ingman","year":"2000","journal-title":"Nature"},{"key":"10.1016\/j.ijcard.2007.02.049_bib21","doi-asserted-by":"crossref","first-page":"671","DOI":"10.1086\/377718","article-title":"Phylogeny of East Asian mitochondrial DNA lineages inferred from complete sequences","volume":"73","author":"Kong","year":"2003","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib22","doi-asserted-by":"crossref","first-page":"1034","DOI":"10.1126\/science.1109792","article-title":"Single, rapid coastal settlement of Asia revealed by analysis of complete mitochondrial genomes","volume":"308","author":"Macaulay","year":"2005","journal-title":"Science"},{"key":"10.1016\/j.ijcard.2007.02.049_bib23","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1007\/s00414-004-0427-6","article-title":"Single nucleotide polymorphisms over the entire mtDNA genome that increase the power of forensic testing in Caucasians","volume":"118","author":"Coble","year":"2004","journal-title":"Int J Legal Med"},{"key":"10.1016\/j.ijcard.2007.02.049_bib24","doi-asserted-by":"crossref","first-page":"1475","DOI":"10.1086\/320591","article-title":"Phylogenetic network for European mtDNA","volume":"68","author":"Finnil\u00e4","year":"2001","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib25","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1111\/j.1529-8817.2005.00222.x","article-title":"Mitochondrial DNA diversity in the Polish Roma","volume":"70","author":"Malyarchuk","year":"2006","journal-title":"Ann Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib26","doi-asserted-by":"crossref","first-page":"26","DOI":"10.1186\/1471-2148-5-26","article-title":"Phylogeny and antiquity of M macrohaplogroup inferred from complete mt DNA sequence of Indian specific lineages","volume":"5","author":"Rajkumar","year":"2005","journal-title":"BMC Evol Biol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib27","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1016\/j.tig.2006.04.001","article-title":"Harvesting the fruit of the human mtDNA tree","volume":"22","author":"Torroni","year":"2006","journal-title":"Trends Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib28","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1007\/s100480050029","article-title":"Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease","volume":"1","author":"K\u00f6sel","year":"1998","journal-title":"Neurogenetics"},{"key":"10.1016\/j.ijcard.2007.02.049_bib29","doi-asserted-by":"crossref","first-page":"1503","DOI":"10.1016\/j.bbrc.2004.10.199","article-title":"Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation","volume":"325","author":"Zhao","year":"2004","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.ijcard.2007.02.049_bib30","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1016\/j.mito.2005.03.003","article-title":"A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy","volume":"5","author":"Povalko","year":"2005","journal-title":"Mitochondrion"},{"key":"10.1016\/j.ijcard.2007.02.049_bib31","doi-asserted-by":"crossref","first-page":"910","DOI":"10.1086\/425590","article-title":"The molecular dissection of mtDNA haplogroup H confirms that the Franco\u2013Cantabrian glacial refuge was a major source for the European gene pool","volume":"75","author":"Achilli","year":"2004","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib32","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1186\/1471-2156-2-13","article-title":"Major genomic mitochondrial lineages delineate early human expansions","volume":"2","author":"Maca-Meyer","year":"2001","journal-title":"BMC Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib33","doi-asserted-by":"crossref","first-page":"1506","DOI":"10.1093\/molbev\/msi142","article-title":"Expanding Southwest Pacific mitochondrial haplogroups P and Q","volume":"22","author":"Friedlaender","year":"2005","journal-title":"Mol Biol Evol"},{"key":"10.1016\/j.ijcard.2007.02.049_bib34","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1007\/s10048-006-0049-x","article-title":"Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL","volume":"7","author":"Annunen-Rasila","year":"2006","journal-title":"Neurogenetics"},{"key":"10.1016\/j.ijcard.2007.02.049_bib35","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1086\/500307","article-title":"The matrilineal ancestry of Ashkenazi jewry: portrait of a recent founder event","volume":"78","author":"Behar","year":"2006","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.ijcard.2007.02.049_bib36","doi-asserted-by":"crossref","first-page":"532","DOI":"10.1073\/pnas.92.2.532","article-title":"Recent African origin of modern humans revealed by complete sequences of hominoid mitochondrial DNAs","volume":"92","author":"Horai","year":"1995","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.ijcard.2007.02.049_bib37","doi-asserted-by":"crossref","first-page":"13034","DOI":"10.1073\/pnas.0506195102","article-title":"Ancient mitochondrial M haplogroups identified in the Southwest Pacific","volume":"102","author":"Merriwether","year":"2005","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.ijcard.2007.02.049_bib38","doi-asserted-by":"crossref","first-page":"6336","DOI":"10.1038\/sj.onc.1209649","article-title":"Nuclear-mitochondrial genomic profiling reveals a pattern of evolution in epithelial ovarian tumor stem cells","volume":"25","author":"Wani","year":"2006","journal-title":"Oncogene"},{"key":"10.1016\/j.ijcard.2007.02.049_bib39","doi-asserted-by":"crossref","first-page":"719","DOI":"10.1073\/pnas.0408894102","article-title":"mtDNA mutations increase tumorigenicity in prostate cancer","volume":"102","author":"Petros","year":"2005","journal-title":"Proc Natl Acad Sci U S A"}],"container-title":["International Journal of Cardiology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527307006341?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0167527307006341?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,28]],"date-time":"2025-09-28T20:21:49Z","timestamp":1759090909000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0167527307006341"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,6]]},"references-count":39,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2008,6]]}},"alternative-id":["S0167527307006341"],"URL":"https:\/\/doi.org\/10.1016\/j.ijcard.2007.02.049","relation":{},"ISSN":["0167-5273"],"issn-type":[{"type":"print","value":"0167-5273"}],"subject":[],"published":{"date-parts":[[2008,6]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The search of \u2018novel\u2019 mtDNA mutations in hypertrophic cardiomyopathy: MITOMAPping as a risk factor","name":"articletitle","label":"Article Title"},{"value":"International Journal of Cardiology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ijcard.2007.02.049","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2007 Elsevier Ireland Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}