{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T07:27:36Z","timestamp":1791098856638,"version":"4.1.0"},"reference-count":13,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2014,8,3]],"date-time":"2014-08-03T00:00:00Z","timestamp":1407024000000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["BMC Neurol"],"published-print":{"date-parts":[[2014,12]]},"DOI":"10.1186\/s12883-014-0156-5","type":"journal-article","created":{"date-parts":[[2014,8,2]],"date-time":"2014-08-02T16:05:37Z","timestamp":1406995537000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report"],"prefix":"10.1186","volume":"14","author":[{"given":"Yuan","family":"Zhao","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yanchen","family":"Xie","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaoquan","family":"Zhu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Huigang","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yao","family":"Li","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jimei","family":"Li","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2014,8,3]]},"reference":[{"key":"156_CR1","doi-asserted-by":"publisher","first-page":"486","DOI":"10.1002\/(SICI)1096-8628(19960614)63:3<486::AID-AJMG14>3.0.CO;2-I","volume":"63","author":"V Ionasescu","year":"1996","unstructured":"Ionasescu V, Ionasescu R, Searby C: Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy. Am J Med Genet. 1996, 63: 486-491. 10.1002\/(SICI)1096-8628(19960614)63:3<486::AID-AJMG14>3.0.CO;2-I.","journal-title":"Am J Med Genet"},{"key":"156_CR2","doi-asserted-by":"crossref","first-page":"8281","DOI":"10.1523\/JNEUROSCI.15-12-08281.1995","volume":"15","author":"SS Scherer","year":"1995","unstructured":"Scherer SS, Desch\u00eanes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL: Connexin 32 a myelin-related protein in the PNS and CNS. J Neurosci. 1995, 15: 8281-8294.","journal-title":"J Neurosci"},{"issue":"2","key":"156_CR3","doi-asserted-by":"publisher","first-page":"142","DOI":"10.1111\/j.1399-0004.2011.01642.x","volume":"81","author":"Y Kim","year":"2012","unstructured":"Kim Y, Choi KG, Park KD, Lee KS, Chung KW, Choi BO: X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans. Clin Genet. 2012, 81 (2): 142-149. 10.1111\/j.1399-0004.2011.01642.x.","journal-title":"Clin Genet"},{"key":"156_CR4","doi-asserted-by":"publisher","first-page":"429","DOI":"10.1002\/ana.10305","volume":"52","author":"HL Paulson","year":"2002","unstructured":"Paulson HL, Garbern JY, Hoban TF, Krajewski KM, Lewis RA, Fischbeck KH, Grossman RI, Lenkinski R, Kamholz JA, Shy ME: Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease. Ann Neurol. 2002, 52: 429-434. 10.1002\/ana.10305.","journal-title":"Ann Neurol"},{"issue":"7","key":"156_CR5","doi-asserted-by":"publisher","first-page":"677","DOI":"10.1111\/j.1469-8749.2010.03674.x","volume":"52","author":"G Anand","year":"2010","unstructured":"Anand G, Maheshwari N, Roberts D, Padeniya A, Hamilton-Ayers M, van der Knaap M, Fratter C, Jayawant S: X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode. Dev Med Child Neurol. 2010, 52 (7): 677-679. 10.1111\/j.1469-8749.2010.03674.x.","journal-title":"Dev Med Child Neurol"},{"key":"156_CR6","doi-asserted-by":"publisher","first-page":"1023","DOI":"10.2169\/internalmedicine.46.0047","volume":"46","author":"R Basri","year":"2007","unstructured":"Basri R, Yabe I, Soma H, Matsushima M, Tsuji S, Sasaki H: X-linked Charcot-Marie-Tooth Disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter. Intern Med. 2007, 46: 1023-1027. 10.2169\/internalmedicine.46.0047.","journal-title":"Intern Med"},{"key":"156_CR7","doi-asserted-by":"publisher","first-page":"2007","DOI":"10.1212\/01.WNL.0000038390.29853.46","volume":"59","author":"HJ Schelhaas","year":"2002","unstructured":"Schelhaas HJ, Van Engelen BG, Gabre\u00ebls-Festen AA, Hageman G, Vliegen JH, Van Der Knaap MS, Zwarts MJ: Transient cerebral white matter lesions in a patient with connexin 32 missense mutation. Neurology. 2002, 59: 2007-2008. 10.1212\/01.WNL.0000038390.29853.46.","journal-title":"Neurology"},{"key":"156_CR8","doi-asserted-by":"publisher","first-page":"605","DOI":"10.1001\/archneur.60.4.605","volume":"60","author":"CO Hanemann","year":"2003","unstructured":"Hanemann CO, Bergmann C, Senderek J, Zerres K, Sperfeld AD: Transient, recurrent white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexion 32 mutation. Arch Neurol. 2003, 60: 605-609. 10.1001\/archneur.60.4.605.","journal-title":"Arch Neurol"},{"key":"156_CR9","doi-asserted-by":"publisher","first-page":"1475","DOI":"10.1212\/01.WNL.0000095960.48964.25","volume":"61","author":"RA Taylor","year":"2003","unstructured":"Taylor RA, Simon EM, Marks HG, Scherer SS: The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem. Neurology. 2003, 61: 1475-1478. 10.1212\/01.WNL.0000095960.48964.25.","journal-title":"Neurology"},{"key":"156_CR10","doi-asserted-by":"publisher","first-page":"1672","DOI":"10.1212\/01.wnl.0000186032.06791.94","volume":"65","author":"G Isoardo","year":"2005","unstructured":"Isoardo G, Di Vito N, Nobile M, Benetton G, Fassio F: X-linked Charcot-Marie - Tooth disease and progressive-relapsing central demyelinating disease. Neurology. 2005, 65: 1672-1673. 10.1212\/01.wnl.0000186032.06791.94.","journal-title":"Neurology"},{"key":"156_CR11","doi-asserted-by":"publisher","first-page":"4736","DOI":"10.1523\/JNEUROSCI.0325-09.2009","volume":"29","author":"I Sargiannidou","year":"2009","unstructured":"Sargiannidou I, Vavlitou N, Aristodemou S, Hadjisavvas A, Kyriacou K, Scherer SS, Kleopa KA: Connexin 32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects. J Neurosci. 2009, 29: 4736-4749. 10.1523\/JNEUROSCI.0325-09.2009.","journal-title":"J Neurosci"},{"key":"156_CR12","doi-asserted-by":"publisher","first-page":"90","DOI":"10.1016\/S0022-510X(99)00146-X","volume":"167","author":"J Senderek","year":"1999","unstructured":"Senderek J, Hermanns B, Bergmann C, Boroojerdi B, Bajbouj M, Hungs M, Ramaekers VT, Quasthoff S, Karch D, Schr\u00f6der JM: X-linked dominant Charoot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations. J Neurol Sci. 1999, 167: 90-101. 10.1016\/S0022-510X(99)00146-X.","journal-title":"J Neurol Sci"},{"issue":"6","key":"156_CR13","doi-asserted-by":"publisher","first-page":"803","DOI":"10.1136\/jnnp.66.6.803","volume":"66","author":"W Marques Jr","year":"1999","unstructured":"Marques W, Sweeney JG, Wood NW, Wroe SJ, Marques W: Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. J Neurol Neurosurg Psychiatry. 1999, 66 (6): 803-804. 10.1136\/jnnp.66.6.803.","journal-title":"J Neurol Neurosurg Psychiatry"}],"container-title":["BMC Neurology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/article\/10.1186\/s12883-014-0156-5\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s12883-014-0156-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s12883-014-0156-5","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1186\/s12883-014-0156-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,9,2]],"date-time":"2021-09-02T05:09:28Z","timestamp":1630559368000},"score":1,"resource":{"primary":{"URL":"https:\/\/bmcneurol.biomedcentral.com\/articles\/10.1186\/s12883-014-0156-5"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,8,3]]},"references-count":13,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2014,12]]}},"alternative-id":["156"],"URL":"https:\/\/doi.org\/10.1186\/s12883-014-0156-5","relation":{},"ISSN":["1471-2377"],"issn-type":[{"value":"1471-2377","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,8,3]]},"assertion":[{"value":"25 August 2013","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"24 July 2014","order":2,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"3 August 2014","order":3,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}],"article-number":"156"}}