Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies

Tamar Harel, John N Griffin, Thomas Arbogast, Tanner O Monroe, Flavia Palombo, Marcella Martinelli, Marco Seri, Tommaso Pippucci, Orly Elpeleg, Nicholas Katsanis

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