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American Journal of Medical Genetics Part A, ISSN 1552-4825, 03/2017, Volume 173, Issue 3, pp. 596 - 600
Journal Article
Journal of the American Heart Association, ISSN 2047-9980, 12/2014, Volume 3, Issue 6, pp. e001407 - n/a
Background-The p.Gln554X mutation in desmocollin-2 (DSC2) is prevalent in approximate to 10% of the Hutterite population. While the homozygous mutation causes... 
screening | Hutterite population | risk stratification | arrhythmogenic cardiomyopathy | arrhythmogenic right ventricular cardiomyopathy/dysplasia | ECG | sudden cardiac death | ECG screening | Arrhythmogenic cardiomyopathy | Sudden cardiac death | Arrhythmogenic right ventricular cardiomyopathy/dysplasia | Risk stratification | CARDIAC & CARDIOVASCULAR SYSTEMS | Predictive Value of Tests | Prognosis | Ventricular Function, Left | Humans | Middle Aged | Male | Alberta - epidemiology | Arrhythmogenic Right Ventricular Dysplasia - diagnosis | Arrhythmogenic Right Ventricular Dysplasia - physiopathology | Arrhythmogenic Right Ventricular Dysplasia - genetics | Young Adult | Ethnic Groups - genetics | DNA Mutational Analysis | Ventricular Premature Complexes - diagnosis | Electrocardiography | Tachycardia, Ventricular - genetics | Adult | Female | Retrospective Studies | Desmocollins - genetics | Death, Sudden, Cardiac - ethnology | Tachycardia, Ventricular - ethnology | Genetic Predisposition to Disease | Risk Factors | Ventricular Premature Complexes - ethnology | Stroke Volume | Homozygote | Magnetic Resonance Imaging | Phenotype | Arrhythmogenic Right Ventricular Dysplasia - ethnology | Tachycardia, Ventricular - diagnosis | Adolescent | Heterozygote | Mutation | Ventricular Premature Complexes - genetics | Ventricular Function, Right | Index Medicus
Journal Article
Human Biology, ISSN 0018-7143, 2011, Volume 83, Issue 5, pp. 599 - 609
Journal Article
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 05/2016, Volume 4, Issue 3, pp. 312 - 321
Hutterites, a religious isolate located in North America, have a number of genetic disorders that are unique and/or over‐represented. A diagnostic chip that... 
mutation | chip | Hutterite | carrier screening | array | diagnostic | APEX | MENNONITE | GIRDLE MUSCULAR-DYSTROPHY | IDENTIFICATION | INTELLECTUAL DISABILITY | HETEROGENEITY | GENE | COMMUNITY | FOUNDER MUTATION | GENETICS & HEREDITY | HAPLOTYPE | APEX array | CEREBELLAR HYPOPLASIA | Population | Deoxyribonucleic acid--DNA | Mutation
Journal Article
Journal Article