Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients

Author: Braida Claudia   Stefanatos Rhoda K.A.   Adam Berit   Mahajan Navdeep   Smeets Hubert J.M.   Niel Florence   Goizet Cyril   Arveiler Benoit   Koenig Michel   Lagier-Tourenne Clotilde   Mandel Jean-Louis   Faber Catharina G.   de Die-Smulders Christine E.M.   Spaans Frank   Monckton Darren G.  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.19, Iss.8, 2010-04, pp. : 1399-1412

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