New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)
Titel:
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)
Auteur:
Sallinen, R Vihola, A Bachinski, L.L Huoponen, K Haapasalo, H Hackman, P Zhang, S Sirito, M Kalimo, H Meola, G Horelli-Kuitunen, N Wessman, M Krahe, R Udd, B