Associated Papers
Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes.
Delplancq G et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2020
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Arndt AK et al.
American Journal of Human Genetics, 2013
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