Wells, Q. S., Ausborn, N. L., Funke, B. H., Pfotenhauer, J. P., Fredi, J. L., Baxter, S., . . . Hong, C. C. (2011). Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variant.
Citação norma ChicagoWells, Quinn S., Natalie L. Ausborn, Birgit H. Funke, Jean P. Pfotenhauer, Joseph L. Fredi, Samantha Baxter, Thomas D. DiSalvo, and Charles C. Hong. Familial Dilated Cardiomyopathy Associated With Congenital Defects in the Setting of a Novel VCL Mutation (Lys815Arg) in Conjunction With a Known MYPBC3 Variant. 2011.
MLA引文Wells, Quinn S., et al. Familial Dilated Cardiomyopathy Associated With Congenital Defects in the Setting of a Novel VCL Mutation (Lys815Arg) in Conjunction With a Known MYPBC3 Variant. 2011.