Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Weidong Jin
Novel Trigenic CACNA1C/DES/MYPN Mutations in a Family of Hypertrophic Cardiomyopathy With Early Repolarization and Short QT Syndrome
Journal of Translational Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Related publications
Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome
Circulation: Cardiovascular Genetics
Detection of Mutations in Symptomatic Patients With Hypertrophic Cardiomyopathy in Taiwan
Journal of Cardiology
Cardiovascular Medicine
Cardiology
Two Novel NPHS1 Mutations in a Chinese Family With Congenital Nephrotic Syndrome
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
The Phenotype/Genotype Relation and the Current Status of Genetic Screening in Hypertrophic Cardiomyopathy, Marfan Syndrome, and the Long QT Syndrome.
Heart
Cardiovascular Medicine
Cardiology
Ehlers-Danlos Syndrome Associated With Cardiomyopathy Hypertrophic Obstructive
Anais Brasileiros de Dermatologia
Dermatology
Association of Takotsubo Cardiomyopathy and Long QT Syndrome
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Novel Calmodulin Mutations Associated With Congenital Long QT Syndrome Affect Calcium Current in Human Cardiomyocytes
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Association of a Congenital Long QT Syndrome Type 1 With Takotsubo Cardiomyopathy
Clinical Case Reports
Medicine
Erratum To: Hypertrophic Cardiomyopathy: Preclinical and Early Phenotype
Journal of Cardiovascular Translational Research
Genetics
Pharmaceutical Science
Cardiovascular Medicine
Molecular Medicine
Cardiology
