{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,10]],"date-time":"2024-02-10T00:21:43Z","timestamp":1707524503131},"reference-count":6,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,12,20]]},"DOI":"10.7759\/cureus.20531","type":"journal-article","created":{"date-parts":[[2021,12,20]],"date-time":"2021-12-20T13:13:30Z","timestamp":1640006010000},"source":"Crossref","is-referenced-by-count":0,"title":["Late-Onset Dystrophinopathy"],"prefix":"10.7759","author":[{"given":"Ranjan K","family":"Singh","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0255011","article-title":"Clinical and genetic spectra in patients with dystrophinopathy in Korea: a single-center study","volume":"16","author":"Yun U","year":"2021","unstructured":"Yun U, Lee SA, Choi WA, et al.. Clinical and genetic spectra in patients with dystrophinopathy in Korea: a single-center study. PLoS One. 2021, 16:e0255011. 10.1371\/journal.pone.0255011","journal-title":"PLoS One"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.4330\/wjc.v8.i6.356","article-title":"Cardiomyopathy in Becker muscular dystrophy: overview","volume":"8","author":"Ho R","year":"2016","unstructured":"Ho R, Nguyen ML, Mather P. Cardiomyopathy in Becker muscular dystrophy: overview. World J Cardiol. 2016, 8:356-61. 10.4330\/wjc.v8.i6.356","journal-title":"World J Cardiol"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1161\/01.cir.94.12.3168","article-title":"Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy","volume":"94","author":"Melacini P","year":"1996","unstructured":"Melacini P, Fanin M, Danieli GA, et al.. Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy. Circulation. 1996, 94:3168-75. 10.1161\/01.cir.94.12.3168","journal-title":"Circulation"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/j.ncl.2014.05.002","article-title":"Duchenne and Becker muscular dystrophies","volume":"32","author":"Flanigan KM","year":"2014","unstructured":"Flanigan KM. Duchenne and Becker muscular dystrophies. Neurol Clin. 2014, 32:671-88. 10.1016\/j.ncl.2014.05.002","journal-title":"Neurol Clin"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1002\/humu.20367","article-title":"Duplications in the DMD gene","volume":"27","author":"White SJ","year":"2006","unstructured":"White SJ, Aartsma-Rus A, Flanigan KM, et al.. Duplications in the DMD gene. Hum Mutat. 2006, 27:938-45. 10.1002\/humu.20367","journal-title":"Hum Mutat"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1136\/jmedgenet-2015-103387","article-title":"The importance of genetic diagnosis for Duchenne muscular dystrophy","volume":"53","author":"Aartsma-Rus A","year":"2016","unstructured":"Aartsma-Rus A, Ginjaar IB, Bushby K. The importance of genetic diagnosis for Duchenne muscular dystrophy. J Med Genet. 2016, 53:145-51. 10.1136\/jmedgenet-2015-103387","journal-title":"J Med Genet"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/80618-late-onset-dystrophinopathy","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:34:50Z","timestamp":1707507290000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/80618-late-onset-dystrophinopathy"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,12,20]]},"references-count":6,"URL":"https:\/\/doi.org\/10.7759\/cureus.20531","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,12,20]]}}}