Author Details

Baxter, Samantha, Laboratory for Molecular Medicine, Partners HealthCare Center for Personalized Genetic Medicine, Cambridge, MA, United States

  • Vol 1, No 1 (2011) - Brief Reports
    Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant
    Abstract  PDF


 
 
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