Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant
Wells, Quinn S., Ausborn, Natalie L., Funke, Birgit H., Pfotenhauer, Jean P., Fredi, Joseph L., Baxter, Samantha, DiSalvo, Thomas G., Hong, Charles C.Volume:
1
Language:
english
Journal:
Cardiogenetics
DOI:
10.4081/cardiogenetics.2011.e10
Date:
August, 2011
File:
PDF, 449 KB
english, 2011