共 82 条
[1]
Ionasescu V(1996)Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy Am J Med Genet 63 486-491
[2]
Ionasescu R(1995)Connexin 32 a myelin-related protein in the PNS and CNS J Neurosci 15 8281-8294
[3]
Searby C(2012)X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans Clin Genet 81 142-149
[4]
Scherer SS(2002)Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease Ann Neurol 52 429-434
[5]
Deschênes SM(2010)X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode Dev Med Child Neurol 52 677-679
[6]
Xu YT(2007)X-linked Charcot-Marie-Tooth Disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter Intern Med 46 1023-1027
[7]
Grinspan JB(2002)Transient cerebral white matter lesions in a patient with connexin 32 missense mutation Neurology 59 2007-2008
[8]
Fischbeck KH(2003)Transient, recurrent white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexion 32 mutation Arch Neurol 60 605-609
[9]
Paul DL(2003)The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem Neurology 61 1475-1478
[10]
Kim Y(2005)X-linked Charcot-Marie - Tooth disease and progressive-relapsing central demyelinating disease Neurology 65 1672-1673