A common missense variant in the neuregulin 1 gene is associated with both schizophrenia and sudden cardiac death

Heart Rhythm

Volumn 10, Issue 7, 2013, Pages 994-998

  Huertas Vazquez, Adriana ^a   Teodorescu, Carmen ^a   Reinier, Kyndaron ^a   Uy Evanado, Audrey ^a   Chugh, Harpriya ^a   Jerger, Katherine ^a   Ayala, Jo ^a   Gunson, Karen ^b   Jui, Jonathan ^c   Newton Cheh, Christopher ^d   Albert, Christine M ^e   Chugh, Sumeet S ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

^b Pathology ^*  (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Association study; Epilepsy; Genetic; Neuregulin 1; Schizophrenia; Sudden cardiac death

Indexed keywords

METHIONINE; NEU DIFFERENTIATION FACTOR; THREONINE;

ADULT; ALLELE; ARTICLE; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART VENTRICLE FIBRILLATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; SUDDEN CARDIAC DEATH;

DEATH, SUDDEN, CARDIAC; DNA; DNA MUTATIONAL ANALYSIS; FOLLOW-UP STUDIES; GENOTYPE; INCIDENCE; MUTATION, MISSENSE; NEUREGULIN-1; OREGON; PROSPECTIVE STUDIES; SCHIZOPHRENIA; VENTRICULAR FIBRILLATION;

EID: 84879501615     PISSN: 15475271     EISSN: 15563871     Source Type: Journal    
DOI: 10.1016/j.hrthm.2013.03.020     Document Type: Article

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