{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T12:38:17Z","timestamp":1756384697152},"reference-count":11,"publisher":"Oxford University Press (OUP)","issue":"919","license":[{"start":{"date-parts":[[2002,5,1]],"date-time":"2002-05-01T00:00:00Z","timestamp":1020211200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2002,5,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Cardiomyopathies are a clinically and genetically heterogeneous group of cardiac diseases in which the myocardium is primarily involved. Mitochondrial DNA point mutations have been identified in a broad spectrum of mitochondrial disorders, which are associated with neurological diseases. However, they also have been reported in patients with cardiomyopathy, either alone or as part of a multisystem disorder. A patient who presented with severe heart failure and was diagnosed as having a mitochondrial A3243G mutation is described.<\/jats:p>","DOI":"10.1136\/pmj.78.919.298","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T10:46:58Z","timestamp":1027766818000},"page":"298-299","source":"Crossref","is-referenced-by-count":12,"title":["Progressive cardiomyopathy as manifestation of mitochondrial disease"],"prefix":"10.1093","volume":"78","author":[{"given":"D N","family":"Nan","sequence":"first","affiliation":[{"name":"Department of Internal Medicine, University Hospital Marqu\u00e9s de Valdecilla , Santander, Cantabria , Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Fern\u00e1ndez-Ayala","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University Hospital Marqu\u00e9s de Valdecilla , Santander, Cantabria , Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Infante","sequence":"additional","affiliation":[{"name":"Service of Neurology"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P","family":"Matorras","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University Hospital Marqu\u00e9s de Valdecilla , Santander, Cantabria , Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Gonz\u00e1lez-Mac\u00edas","sequence":"additional","affiliation":[{"name":"Department of Internal Medicine, University Hospital Marqu\u00e9s de Valdecilla , Santander, Cantabria , Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2002,5,1]]},"reference":[{"key":"2023042416172226800_R1","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1016\/S0733-8619(18)30832-6","article-title":"Mitocondrial 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