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CIRCGENETICS.116.001431
CIRCGENETICS.116.001431
http://dx.doi.org/10.1161/CIRCGENETICS.116.001431
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction.
P356
Q37346547-DF5ADDEF-086E-4AFE-8354-5B1BFACDAA1B
P356
CIRCGENETICS.116.001431
http://dx.doi.org/10.1161/CIRCGENETICS.116.001431