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However, muscle biopsy showed massive accumulation of glycogen, although no significant abnormality of glycolytic pathway enzymes could be demonstrated. This patient therefore has a previously undescribed myopathy associated with both Becker muscular dystrophy and a glycogen storage disorder of unknown aetiology. \u00a9 1993 John Wiley &amp; Sons, Inc.<\/jats:p>","DOI":"10.1002\/mus.880160110","type":"journal-article","created":{"date-parts":[[2005,1,1]],"date-time":"2005-01-01T10:40:34Z","timestamp":1104576034000},"page":"57-62","source":"Crossref","is-referenced-by-count":3,"title":["A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage"],"prefix":"10.1002","volume":"16","author":[{"given":"Michael R.","family":"Rose","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robin S.","family":"Howard","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sally A.","family":"Genet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catherine J.","family":"McMahon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.","family":"Whitfield","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John A.","family":"Morgan\u2010Hughes","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2004,10,13]]},"reference":[{"key":"e_1_2_1_2_2","doi-asserted-by":"publisher","DOI":"10.1002\/mus.880030602"},{"key":"e_1_2_1_3_2","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.86.18.7154"},{"key":"e_1_2_1_4_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00205170"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1002\/mus.880010204"},{"key":"e_1_2_1_6_2","first-page":"A179","article-title":"Characterisation of Duchenne muscular dystrophy patients with antisera which recognise the amino and carboxy\u2010terminal regions of dystrophin","volume":"45","author":"Bulman DE","year":"1989","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/0026-0495(87)90113-2"},{"key":"e_1_2_1_8_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00313831"},{"key":"e_1_2_1_9_2","first-page":"612","article-title":"Normal human genomic restriction fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA","volume":"43","author":"Darras BT","year":"1988","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_10_2","first-page":"126","article-title":"Myopathy in complex glycerol kinase deficiency patients is due to 3\u2032 deletions of the dystrophin gene","volume":"43","author":"Darras BT","year":"1988","journal-title":"Am J Hum Genet"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410270521"},{"key":"e_1_2_1_12_2","first-page":"1619","volume-title":"Myology","author":"DiMauro S","year":"1986"},{"key":"e_1_2_1_13_2","volume-title":"Muscle Biopsy: A Practical Approach","author":"Dubowitz V","year":"1985"},{"key":"e_1_2_1_14_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1976.tb00033.x"},{"key":"e_1_2_1_15_2","doi-asserted-by":"publisher","DOI":"10.1016\/0022-510X(83)90144-2"},{"key":"e_1_2_1_16_2","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410260202"},{"key":"e_1_2_1_17_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.39.10.1277"},{"key":"e_1_2_1_18_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.31.9.1077"},{"key":"e_1_2_1_19_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.39.8.1011"},{"key":"e_1_2_1_20_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.19.6.553"},{"key":"e_1_2_1_21_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00687012"},{"key":"e_1_2_1_22_2","doi-asserted-by":"publisher","DOI":"10.1172\/JCI113890"},{"key":"e_1_2_1_23_2","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320360106"},{"key":"e_1_2_1_24_2","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1016\/S0733-8619(18)30833-8","article-title":"Disorders of glycogen metablism of muscle","volume":"7","author":"Servidei S","year":"1989","journal-title":"Neurol Clin"},{"key":"e_1_2_1_25_2","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410280506"},{"key":"e_1_2_1_26_2","doi-asserted-by":"publisher","DOI":"10.1002\/mus.880110411"},{"key":"e_1_2_1_27_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(05)80545-1"},{"key":"e_1_2_1_28_2","doi-asserted-by":"publisher","DOI":"10.1016\/0888-7543(90)90181-S"},{"key":"e_1_2_1_29_2","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/108.4.845"},{"key":"e_1_2_1_30_2","first-page":"519","volume-title":"Disorders of Voluntary Muscle","author":"Walton J","year":"1988"}],"container-title":["Muscle &amp; 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