DOI:
10.1055/s-00000004
Aktuelle Neurologie
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References
Saalinen R, Vihola A, Bachinski LL. et al.
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
Neuromuscul Disord 2004; 14: 274-283
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