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These results exclude the presence of deletions or insertions of greater than 60 bp in the region of the mitochondrial genome examined. Any causative mitochondrial DNA mutations in these disorders are therefore likely to be point mutations or small structural rearrangements.<\/jats:p>","DOI":"10.1136\/jmg.25.9.600","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:11:11Z","timestamp":1226329871000},"page":"600-605","source":"Crossref","is-referenced-by-count":7,"title":["Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy."],"prefix":"10.1136","volume":"25","author":[{"given":"J","family":"Poulton","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D M","family":"Turnbull","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A B","family":"Mehta","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Wilson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R M","family":"Gardiner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1988,9,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1093\/brain\/105.3.553","article-title":"Mitochondrial encephalomyopathies","volume":"105","author":"t Morgan-Hughes JA, References; DJ, Hayes; JB, Clark","year":"1982","unstructured":"References t Morgan-Hughes JA, Hayes DJ, Clark JB, et al. 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