Genotype and clinical characteristics of congenital long QT syndrome in Thailand

by Ankavipar Saprungruang, Apichai Khongphatthanayothin, John Mauleekoonphairoj, Pharawee Wandee, Supaluck Kanjanauthai, Zahurul A. Bhuiyan, Arthur A.M. Wilde, Yong Poovorawan
Published 2018-09-01

Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy

by Atiyeh M Abdallah, S. Justin Carlus, Abdulhadi H Al-Mazroea, Mohammad Alluqmani, Yousef Almohammadi, Zahurul A Bhuiyan, Khalid M Al-Harbi
Published 2019-01-01

A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of...

by Sven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, Antonius Baartscheer, Lars Eckardt, Matthias Paul, Carol Ann Remme, Zahurul A Bhuiyan, Connie R Bezzina, Eric Schulze-Bahr
Published 2013-01-01

ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy

by Jean-Marc Good, MD, PhD, Florence Fellmann, MD, PhD, Zahurul A. Bhuiyan, MBBS, PhD, FESC, Samuel Rotman, MD, Etienne Pruvot, MD, Jürg Schläpfer, MD
Published 2020-01-01