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New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

Author:
R Sallinen   A Vihola   L.L Bachinski   K Huoponen   H Haapasalo   P Hackman   S Zhang   M Sirito   H Kalimo   G Meola   N Horelli-Kuitunen   M Wessman   R Krahe   B Udd  


Issue Date:
2004


Abstract(summary):

http://linkinghub.elsevier.com/retrieve/pii/S0960896604000082


Page:
0-283


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