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6. [A sporadic case of Charcot-Marie-Tooth disease type 1 A associated with a duplication in chromosome 17 p11.2-p12]. Inoue M; Kojima M; Aikoh H; Sugai K; Murakami N; Nonaka I; Hayasaka K; Yamamoto M; Sobue G No To Hattatsu; 1999 Sep; 31(5):452-7. PubMed ID: 10487071 [TBL] [Abstract][Full Text] [Related]
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8. Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group. Brice A; Ravisé N; Stevanin G; Gugenheim M; Bouche P; Penet C; Agid Y J Med Genet; 1992 Nov; 29(11):807-12. PubMed ID: 1453432 [TBL] [Abstract][Full Text] [Related]
10. Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease. LeGuern E; Gouider R; Mabin D; Tardieu S; Birouk N; Parent P; Bouche P; Brice A Ann Neurol; 1997 Jan; 41(1):104-8. PubMed ID: 9005872 [TBL] [Abstract][Full Text] [Related]
11. [Molecular pathology of Charcot-Marie-Tooth disease type 1A: abnormal expression of PMP-22]. Yoshikawa H; Nishimura T; Yanagihara T Rinsho Shinkeigaku; 1995 Dec; 35(12):1441-3. PubMed ID: 8752424 [TBL] [Abstract][Full Text] [Related]
12. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. Wise CA; Garcia CA; Davis SN; Heju Z; Pentao L; Patel PI; Lupski JR Am J Hum Genet; 1993 Oct; 53(4):853-63. PubMed ID: 8105684 [TBL] [Abstract][Full Text] [Related]
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14. Longitudinal studies of the duplication form of Charcot-Marie-Tooth polyneuropathy. Killian JM; Tiwari PS; Jacobson S; Jackson RD; Lupski JR Muscle Nerve; 1996 Jan; 19(1):74-8. PubMed ID: 8538673 [TBL] [Abstract][Full Text] [Related]
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18. Nerve conduction velocity in CMT1A: what else can we tell? Manganelli F; Pisciotta C; Reilly MM; Tozza S; Schenone A; Fabrizi GM; Cavallaro T; Vita G; Padua L; Gemignani F; Laurà M; Hughes RA; Solari A; Pareyson D; Santoro L; Eur J Neurol; 2016 Oct; 23(10):1566-71. PubMed ID: 27412484 [TBL] [Abstract][Full Text] [Related]