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Abbreviation : CMT1
Long Form : Charcot-Marie-Tooth type 1 disease
No. Year Title Co-occurring Abbreviation
2007 [Mutations in the mitofusin 2 gene are the most common cause of Charcot-Marie-Tooth type 2 disease]. ---
2004 Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene. CHN, CMT, MPZ
2002 Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type I disease. ECM
1998 Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPP. HNPP, PMP22
1997 Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. CMT1A, HNPP