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The authors describe a novel mutation (mt. 15209T&gt;C) in mitochondrial cytochrome b gene in a 2-year-old girl with Prader-Willi syndrome with a clinical history of lactic acidosis attacks, renal sodium loss, hepatopathy, progressive cerebral atrophy, and sudden death. The authors suggest that atypical clinical findings in patients with Prader-Willi syndrome should direct the physician to search for a mitochondrial disease.<\/jats:p>","DOI":"10.1177\/0883073814530499","type":"journal-article","created":{"date-parts":[[2014,4,25]],"date-time":"2014-04-25T23:33:18Z","timestamp":1398468798000},"page":"378-381","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":3,"title":["A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (\n                    <i>MTCYB<\/i>\n                    ) in a Patient with Prader Willi Syndrome"],"prefix":"10.1177","volume":"30","author":[{"given":"Ulu\u00e7","family":"Yi\u015f","sequence":"first","affiliation":[{"name":"Department of Pediatrics, Division of Child Neurology, Dokuz Eyl\u00fcl University, School of Medicine, \u0130zmir, Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fatih 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