DOI:
10.1055/s-00000004
Aktuelle Neurologie
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References
Bachinski LL, Udd B, Meola G. et al.
Confirmation of DM2 (CCTG)n expansion mutation in PROMM/PDM patients of different European origins: a single shared haplotype indicates ancestral founder effects.
Am J Hum Genet 2003; 73: 835-848
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