SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype.

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Bibliographic Details
Title: SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype.
Authors: Bugiardini, E.1, Rivolta, I.2, Binda, A.2, Soriano Caminero, A.3, Cirillo, F.4, Cinti, A.5, Giovannoni, R.5, Botta, A.6, Cardani, R.7, Wicklund, M.P.3, Meola, G.1,7 giovanni.meola@unimi.it
Source: Neuromuscular Disorders. Apr2015, Vol. 25 Issue 4, p301-307. 7p.
Database: Academic Search Ultimate
Description
ISSN:09608966
DOI:10.1016/j.nmd.2015.01.006