{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T12:57:43Z","timestamp":1788872263547,"version":"build-2803163510"},"reference-count":9,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2012,8,1]],"date-time":"2012-08-01T00:00:00Z","timestamp":1343779200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2016,1,27]],"date-time":"2016-01-27T00:00:00Z","timestamp":1453852800000},"content-version":"vor","delay-in-days":1274,"URL":"https:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics & Neonatology"],"published-print":{"date-parts":[[2012,8]]},"DOI":"10.1016\/j.pedneo.2011.08.013","type":"journal-article","created":{"date-parts":[[2012,7,21]],"date-time":"2012-07-21T01:40:28Z","timestamp":1342834828000},"page":"264-268","source":"Crossref","is-referenced-by-count":15,"title":["A Novel 3670-Base Pair Mitochondrial DNA Deletion Resulting in Multi-systemic Manifestations in a Child"],"prefix":"10.1016","volume":"53","author":[{"given":"Hsin-Ming","family":"Liu","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li-Ping","family":"Tsai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yin-Hsiu","family":"Chien","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jia-Feng","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wen-Chin","family":"Weng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shinn-Forng","family":"Peng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"En-Ting","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pei-Hsin","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wang-Tso","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"I-Jun","family":"Tsai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wuh-Liang","family":"Hwu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ni-Chung","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.pedneo.2011.08.013_bib1","series-title":"MITOMAP: a human mitochondrial genome database","author":"Ruiz-Pesini","year":"2010"},{"key":"10.1016\/j.pedneo.2011.08.013_bib2","series-title":"Mitochondrial disorders overview","author":"Chinnery","year":"1993"},{"key":"10.1016\/j.pedneo.2011.08.013_bib3","series-title":"Mitochondrial DNA deletion syndromes GeneReviews","author":"DiMauro","year":"2007"},{"key":"10.1016\/j.pedneo.2011.08.013_bib4","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1097\/00125817-200111000-00004","article-title":"Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation","volume":"3","author":"Wong","year":"2001","journal-title":"Genet Med"},{"key":"10.1016\/j.pedneo.2011.08.013_bib5","doi-asserted-by":"crossref","first-page":"e15687","DOI":"10.1371\/journal.pone.0015687","article-title":"Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes","volume":"5","author":"Sadikovic","year":"2010","journal-title":"PLoS One"},{"key":"10.1016\/j.pedneo.2011.08.013_bib6","doi-asserted-by":"crossref","first-page":"449","DOI":"10.1016\/j.mito.2010.04.003","article-title":"A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles","volume":"10","author":"Mkaouar-Rebai","year":"2010","journal-title":"Mitochondrion"},{"key":"10.1016\/j.pedneo.2011.08.013_bib7","doi-asserted-by":"crossref","first-page":"1406","DOI":"10.1212\/01.WNL.0000033795.17156.00","article-title":"Diagnostic criteria for respiratory chain disorders in adults and children","volume":"59","author":"Bernier","year":"2002","journal-title":"Neurology"},{"key":"10.1016\/j.pedneo.2011.08.013_bib8","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1016\/j.ymgme.2008.04.004","article-title":"The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle","volume":"94","author":"Brautbar","year":"2008","journal-title":"Mol Genet Metab"},{"key":"10.1016\/j.pedneo.2011.08.013_bib9","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1136\/jmg.40.3.188","article-title":"The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency","volume":"40","author":"Chol","year":"2003","journal-title":"J Med Genet"}],"container-title":["Pediatrics & Neonatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S187595721200071X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S187595721200071X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,11,22]],"date-time":"2018-11-22T01:20:14Z","timestamp":1542849614000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S187595721200071X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,8]]},"references-count":9,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2012,8]]}},"alternative-id":["S187595721200071X"],"URL":"https:\/\/doi.org\/10.1016\/j.pedneo.2011.08.013","relation":{},"ISSN":["1875-9572"],"issn-type":[{"value":"1875-9572","type":"print"}],"subject":[],"published":{"date-parts":[[2012,8]]}}}