Cite
HARVARD Citation
Brodehl, A. et al. (2020). A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. Journal of molecular and cellular cardiology. pp. 17-29. [Online].
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Brodehl, A. et al. (2020). A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. Journal of molecular and cellular cardiology. pp. 17-29. [Online].