Role of CAMK2D in neurodevelopment and associated conditions
Pomme M.F. Rigter, Charlotte de Konink, Matthew J. Dunn, Martina Proietti Onori, Jennifer B. Humberson, Matthew Thomas, Caitlin Barnes, Carlos E. Prada, K. Nicole Weaver, Thomas D. Ryan, Oana Caluseriu, Jennifer Conway, Emily Calamaro, Chin‐To Fong, Wim Wuyts, Marije Meuwissen, Eva Hordijk, Carsten N. Jonkers, Lucas A. Anderson, Berfin Yuseinova, Sarah Polonia, Diane Beysen, Zornitza Stark, Elena Savva, Cathryn Poulton, F. Ellis McKenzie, Elizabeth Bhoj, Caleb Bupp, Stéphane Bezieau, Sandra Mercier, Amy Blevins, Ingrid M. Wentzensen, Fan Xia, Jill A. Rosenfeld, Tzung‐Chien Hsieh, Peter Krawitz, Miriam Elbracht, Danielle Veenma, Howard Schulman, Margaret M. Stratton, Sébastien Küry, Geeske M. van Woerden
Topics & Concepts
Gene isoformNeurodevelopmental disorderIsozymeLoss functionCardiomyopathyIntellectual disabilityGeneticsBiologyGeneDilated cardiomyopathyNeuroscienceMedicinePhenotypeInternal medicineHeart failureEnzymeBiochemistryCardiomyopathy and Myosin StudiesCongenital heart defects researchGenetics and Neurodevelopmental Disorders