Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome

Author:

Barrett Karlene T1,Rodikova Ekaterina1,Weese-Mayer Debra E2,Rand Casey M2,Marazita Mary L3,Cooper Margaret E3,Berry-Kravis Elizabeth M4,Bech-Hansen N Torben5,Wilson Richard JA1

Affiliation:

1. Department of Physiology and Pharmacology; Hotchkiss Brain Institute and Alberta Children's Hospital Research Institute; University of Calgary; Calgary AB Canada

2. Center for Autonomic Medicine in Pediatrics; Ann & Robert H. Lurie Children's Hospital of Chicago; Northern University Feinberg School of Medicine; Chicago IL USA

3. Department of Oral Biology; Center for Craniofacial and Dental Genetics; School of Dental Medicine and Department of Human Genetics; University of Pittsburgh; Pittsburgh PA USA

4. Departments of Pediatrics, Neurological Sciences and Biochemistry; Rush University Medical Center; Chicago IL USA

5. Department of Medical Genetics; Alberta Children's Hospital Research Institute; University of Calgary; Calgary AB Canada

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Reference29 articles.

1. Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development;Willinger;Pediatr Pathol,1991

2. Infant mortality statistics from the 2007 period linked birth/infant death data set;Matthews;Natl Vital Stat Rep,2011

3. International trends in sudden infant death syndrome: stabilization of rates requires further action;Hauck;Pediatrics,2008

4. Temporal trends in sudden infant death syndrome in Canada from 1991 to 2005: contribution of changes in cause of death assignment practices and in maternal and infant characteristics;Gilbert;Paediatr Perinat Epidemiol,2012

5. Decades of disparity: widening ethnic mortality gaps from 1980 to 1999;Blakely;N Z Med J,2004

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