{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,23]],"date-time":"2026-01-23T07:58:34Z","timestamp":1769155114880,"version":"3.49.0"},"reference-count":20,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","nmd-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Neuromuscular Disorders"],"published-print":{"date-parts":[[2021,5]]},"DOI":"10.1016\/j.nmd.2021.02.005","type":"journal-article","created":{"date-parts":[[2021,2,10]],"date-time":"2021-02-10T12:12:41Z","timestamp":1612959161000},"page":"456-461","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"title":["A rare case of monozygotic triplets with Duchenne muscular dystrophy"],"prefix":"10.1016","volume":"31","author":[{"given":"Liang","family":"Wang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jinfu","family":"Lin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fu","family":"Xiong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yingyin","family":"Liang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huan","family":"Li","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ziyu","family":"Liao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cheng","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.nmd.2021.02.005_bib0001","doi-asserted-by":"crossref","first-page":"l7012","DOI":"10.1136\/bmj.l7012","article-title":"Duchenne muscular dystrophy","volume":"368","author":"Fox","year":"2020","journal-title":"BMJ"},{"key":"10.1016\/j.nmd.2021.02.005_bib0002","doi-asserted-by":"crossref","first-page":"E1","DOI":"10.1002\/mus.26081","article-title":"Leg muscle MRI in identical twin boys with duchenne muscular dystrophy","volume":"58","author":"Willcocks","year":"2018","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2021.02.005_bib0003","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1002\/ajmg.1320330116","article-title":"Duchenne muscular dystrophy in monozygotic twins: deletion of 5\u2032 fragments of the gene","volume":"33","author":"Ionasescu","year":"1989","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.nmd.2021.02.005_bib0004","doi-asserted-by":"crossref","first-page":"2021","DOI":"10.1016\/j.apmr.2008.03.009","article-title":"Convexity of scoliosis related to handedness in identical twin boys with Duchenne's muscular dystrophy: a case report","volume":"89","author":"Werner","year":"2008","journal-title":"Arch Phys Med Rehabil"},{"key":"10.1016\/j.nmd.2021.02.005_bib0005","doi-asserted-by":"crossref","first-page":"1456","DOI":"10.3945\/ajcn.116.144279","article-title":"Breastfeeding and motor development in term and preterm infants in a longitudinal US cohort","volume":"106","author":"Michels","year":"2017","journal-title":"Am J Clin Nutr"},{"key":"10.1016\/j.nmd.2021.02.005_bib0006","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1016\/S0022-3476(05)80660-2","article-title":"Gross motor milestones in preterm infants: correction for degree of prematurity","volume":"116","author":"Allen","year":"1990","journal-title":"J Pediatr"},{"key":"10.1016\/j.nmd.2021.02.005_bib0007","doi-asserted-by":"crossref","first-page":"269","DOI":"10.1016\/0960-8966(92)90059-F","article-title":"Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability","volume":"2","author":"Hodgson","year":"1992","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.nmd.2021.02.005_bib0008","doi-asserted-by":"crossref","first-page":"836","DOI":"10.1016\/j.clinbiochem.2010.03.014","article-title":"Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD\/BMD patients","volume":"43","author":"Madania","year":"2010","journal-title":"Clin Biochem"},{"key":"10.1016\/j.nmd.2021.02.005_bib0009","doi-asserted-by":"crossref","first-page":"170","DOI":"10.3109\/01677063.2013.830616","article-title":"Exon deletion patterns of the dystrophin gene in 82 Vietnamese Duchenne\/Becker muscular dystrophy patients","volume":"27","author":"Tran","year":"2013","journal-title":"J Neurogenet"},{"key":"10.1016\/j.nmd.2021.02.005_bib0010","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1023\/A:1025824105194","article-title":"Different expressions of X-linked cardiomyopathy in monozygotic triplets with Becker's dystrophy","volume":"19","author":"Chrzanowski","year":"2003","journal-title":"Int J Cardiovasc Imaging"},{"key":"10.1016\/j.nmd.2021.02.005_bib0011","doi-asserted-by":"crossref","first-page":"189","DOI":"10.4414\/smw.2006.11213","article-title":"Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series","volume":"136","author":"Ramelli","year":"2006","journal-title":"Swiss Med Wkly"},{"key":"10.1016\/j.nmd.2021.02.005_bib0012","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1002\/mus.880110402","article-title":"Becker muscular dystrophy recombinant DNA studies in identical twins","volume":"11","author":"Ionasescu","year":"1988","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.nmd.2021.02.005_bib0013","doi-asserted-by":"crossref","first-page":"1332","DOI":"10.1038\/s41556-020-00595-5","article-title":"The lncRNA H19 alleviates muscular dystrophy by stabilizing dystrophin","volume":"22","author":"Zhang","year":"2020","journal-title":"Nat Cell Biol"},{"key":"10.1016\/j.nmd.2021.02.005_bib0014","doi-asserted-by":"crossref","first-page":"e12063","DOI":"10.15252\/emmm.202012063","article-title":"Trans-generational epigenetic regulation associated with the amelioration of Duchenne Muscular Dystrophy","volume":"12","author":"Martone","year":"2020","journal-title":"EMBO Mol Med"},{"key":"10.1016\/j.nmd.2021.02.005_bib0015","doi-asserted-by":"crossref","first-page":"4153","DOI":"10.1016\/j.febslet.2007.07.021","article-title":"Heregulin-induced epigenetic regulation of the utrophin-A promoter","volume":"581","author":"Basu","year":"2007","journal-title":"FEBS Lett"},{"key":"10.1016\/j.nmd.2021.02.005_bib0016","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1177\/0883073818773029","article-title":"Is there a delay in diagnosis of duchenne muscular dystrophy among preterm-born males?","volume":"33","author":"Soim","year":"2018","journal-title":"J Child Neurol"},{"key":"10.1016\/j.nmd.2021.02.005_bib0017","first-page":"55","article-title":"The Northwestern University Triplet Study. I: overview of the international literature","volume":"37","author":"Keith","year":"1988","journal-title":"Acta Genet Med Gemellol (Roma)"},{"key":"10.1016\/j.nmd.2021.02.005_bib0018","doi-asserted-by":"crossref","first-page":"1198","DOI":"10.1111\/dmcn.14623","article-title":"Early developmental milestones in Duchenne muscular dystrophy","volume":"62","author":"van Dommelen","year":"2020","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.nmd.2021.02.005_bib0019","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1111\/j.1469-8749.1986.tb03882.x","article-title":"Language development of term and preterm children during the first five years of life","volume":"28","author":"Largo","year":"1986","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.nmd.2021.02.005_bib0020","first-page":"1150","article-title":"Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk","volume":"51","author":"Passos-Bueno","year":"1992","journal-title":"Am J Hum Genet"}],"container-title":["Neuromuscular Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896621000316?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0960896621000316?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T08:10:33Z","timestamp":1760775033000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0960896621000316"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,5]]},"references-count":20,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2021,5]]}},"alternative-id":["S0960896621000316"],"URL":"https:\/\/doi.org\/10.1016\/j.nmd.2021.02.005","relation":{},"ISSN":["0960-8966"],"issn-type":[{"value":"0960-8966","type":"print"}],"subject":[],"published":{"date-parts":[[2021,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"A rare case of monozygotic triplets with Duchenne muscular dystrophy","name":"articletitle","label":"Article Title"},{"value":"Neuromuscular Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.nmd.2021.02.005","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2021 Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}