Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human
J. Clin. Invest. Kobra Haghighi, et al. 111:869 doi:10.1172/JCI17892 [
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Figure 2Analysis of inheritance of the T116G mutation in kindred II. Pedigree for the presence or absence of the T116G mutation in four generations. Two brothers (probands III-13 and III-14) who were heterozygous for the L39stop mutation presented with a dilated cardiomyopathy. Their deceased father, II-9, was also diagnosed with dilated cardiomyopathy. Squares represent males and circles represent females. A line denotes that the patient is deceased.