Associated Papers
Phenotypic expansion of CALM1/2-associated disorders to include neurologic phenotypes without arrhythmia.
Hoang HD et al.
Human Molecular Genetics, 2025
Calmodulin Mutations in Human Disease.
Hussey JW et al.
Channels (austin, Tex.), 2023
Calmodulin Mutations Associated with Heart Arrhythmia: A Status Report.
Chazin WJ et al.
International Journal of Molecular Sciences, 2020
Select a paper to view details