Cite
HARVARD Citation
Delplancq, G. et al. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American journal of medical genetics. 184 (1), pp. 129-135. [Online].
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Delplancq, G. et al. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American journal of medical genetics. 184 (1), pp. 129-135. [Online].