α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Genetic Variations in Nitric Oxide Synthase 1 Adaptor Protein Are Associated With Sudden Cardiac Death in US White Community-Based Populations

(2009) W.H. Linda Kao et al.   CIRCULATION

Brainstem mechanisms underlying the sudden infant death syndrome: Evidence from human pathologic studies

(2009) Hannah C. Kinney   DEVELOPMENTAL PSYCHOBIOLOGY

What Is the mechanism of SIDS? Clues from epidemiology

(2009) Edwin A. Mitchell   DEVELOPMENTAL PSYCHOBIOLOGY

Genetic Modulation of Brugada Syndrome by a Common Polymorphism

(2009) ERIC LIZOTTE et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

SNP association and sequence analysis of the NOS1AP gene in SIDS

(2009) Motoki Osawa et al.   Legal Medicine

α-1-Syntrophin Mutation and the Long-QT Syndrome

(2008) Geru Wu et al.   Circulation-Arrhythmia and Electrophysiology

Association of NOS1AP Genetic Variants With QT Interval Duration in Families From the Diabetes Heart Study

(2008) A. B. Lehtinen et al.   DIABETES

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration

(2008) M. Eijgelsheim et al.   HUMAN MOLECULAR GENETICS

Cardiac Ion Channel Gene Mutations in Sudden Infant Death Syndrome

(2008) Tesshu Otagiri et al.   PEDIATRIC RESEARCH

CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart

(2008) K.-C. Chang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

(2008) K. Ueda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA