Jimpymsd mouse mutation and connatal Pelizaeus-Merzbacher disease

American Journal of Medical GeneticsVolume 75, Issue 4 p. 439-440 Letter to the Editor Jimpymsd mouse mutation and connatal Pelizaeus-Merzbacher disease Toshiyuki Yamamoto, Corresponding Author Toshiyuki Yamamoto Gene Research Center, Tottori University, Yonago, JapanGene Research Center, Tottori University, 86 Nishi-machi, Yonago 683, Japan. E-mail: [email protected]Search for more papers by this authorEiji Nanba, Eiji Nanba Gene Research Center, Tottori University, Yonago, JapanSearch for more papers by this authorHaidi Zhang, Haidi Zhang Gene Research Center, Tottori University, Yonago, JapanSearch for more papers by this authorMasayuki Sasaki, Masayuki Sasaki Department of Child Neurology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this authorHirohumi Komaki, Hirohumi Komaki Department of Child Neurology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this authorKenzo Takeshita, Kenzo Takeshita Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University, Yonago, JapanSearch for more papers by this author Toshiyuki Yamamoto, Corresponding Author Toshiyuki Yamamoto Gene Research Center, Tottori University, Yonago, JapanGene Research Center, Tottori University, 86 Nishi-machi, Yonago 683, Japan. E-mail: [email protected]Search for more papers by this authorEiji Nanba, Eiji Nanba Gene Research Center, Tottori University, Yonago, JapanSearch for more papers by this authorHaidi Zhang, Haidi Zhang Gene Research Center, Tottori University, Yonago, JapanSearch for more papers by this authorMasayuki Sasaki, Masayuki Sasaki Department of Child Neurology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this authorHirohumi Komaki, Hirohumi Komaki Department of Child Neurology, National Center Hospital for Mental, Nervous, and Muscular Disorders, National Center of Neurology and Psychiatry, Tokyo, JapanSearch for more papers by this authorKenzo Takeshita, Kenzo Takeshita Division of Child Neurology, Institute of Neurological Sciences, Faculty of Medicine, Tottori University, Yonago, JapanSearch for more papers by this author First published: 06 December 1998 https://doi.org/10.1002/(SICI)1096-8628(19980203)75:4<439::AID-AJMG19>3.0.CO;2-PCitations: 22AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES Doll R, Natowicz MR, Schiffmann R, Smith FI (1992): Molecular diagnostics for myelin proteolipid protein gene mutations in Pelizaeus-Merzbacher disease. Am J Hum Genet 51: 161–169. Gow A, Lazzarini RA (1996): A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease. Nat Genet 13: 422–428. Hodes ME, Pratt VM, Dlouhy SR (1993): Genetics of Pelizaeus-Merzbacher disease. Dev Neurosci 15: 383–394. Hudson LD, Puckett C, Berndt J, Chan J, Gencic S (1989): Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder. Proc Natl Acad Sci USA 86: 8128–8131. Kobayashi H, Hoffman EP, Marks HG (1994): The rumpshaker mutation in spastic paraplegia. Nat Genet 7: 351–352. Citing Literature Volume75, Issue43 February 1998Pages 439-440 ReferencesRelatedInformation