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HARVARD Citation
Maruthappu, T. et al. (2019). Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype4. British journal of dermatology. pp. 1114-1122. [Online].
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Maruthappu, T. et al. (2019). Loss‐of‐function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype4. British journal of dermatology. pp. 1114-1122. [Online].