Arrhythmogenic Cardiomyopathy in a Patient With a Rare Loss‐of‐Function <i>KCNQ1</i> Mutation
Qinmei Xiong(Nanchang University), Kui Hong(Nanchang University), Jinyan Xie(Sir Run Run Shaw Hospital), Rong Wan(Shanghai Ninth People's Hospital), Yang Shen(Shanghai Institute of Hematology), Jianhua Yu(Zhejiang Chinese Medical University), Sujuan Yan(Nanchang University), Qing Cao(Ministry of Education of the People's Republic of China), Qiongqiong Zhou(Nanchang University), Ali J. Marian(The University of Texas Health Science Center at Houston)
Cited by 31
Related Papers
RNA demethylase ALKBH5 prevents pancreatic cancer progression by posttranscriptional activation of PER1 in an m6A-YTHDF2-dependent manner
|Molecular Cancer|2020|434
MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II
|Human Molecular Genetics|2007|289
Genetic Fate Mapping Identifies Second Heart Field Progenitor Cells As a Source of Adipocytes in Arrhythmogenic Right Ventricular Cardiomyopathy
|Circulation Research|2009|148
Akkermansia muciniphila protects mice against an emerging tick-borne viral pathogen
|Nature Microbiology|2023|125