Amnah Bdeir YOU? Author Swipe

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Genetic Mosaicism in Calmodulinopathy Open

Lisa M. Wren, Juan Jiménez‐Jáimez, Saleh AlGhamdi, Jumana Y. Al‐Aama, Amnah Bdeir , et al. · 2019

Background: CaM (calmodulin) mutations are associated with congenital arrhythmia susceptibility (calmodulinopathy) and are most often de novo. In this report, we sought to broaden the genotype-phenotype spectrum of calmodulinopathies with …