Clinical and Genetic Characteristics of Arrhythmogenic Right Ventricular Cardiomyopathy Patients: A Single-Center Experience

por Al-Ghamdi, Bandar Saeed, Alhadeq, Faten, Alqahtani, Aisha, Alruwaili, Nadiah, Rababh, Monther, Alghamdi, Sara, Almanea, Waleed, Alhassnan, Zuhair
Publicado 2023

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

por Al-Hassnan, Zuhair N., Shinwari, Zarghuna MA., Wakil, Salma M., Tulbah, Sahar, Mohammed, Shamayel, Rahbeeni, Zuhair, Alghamdi, Mohammed, Rababh, Monther, Colak, Dilek, Kaya, Namik, Al-Fayyadh, Majid, Alburaiki, Jehad
Publicado 2016