Associated Papers
Noncardiac genetic predisposition in sudden infant death syndrome.
Gray B et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population.
Liebrechts-Akkerman G et al.
International Journal of Legal Medicine, 2014
Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.
Paterson DS
Respiratory Physiology & Neurobiology, 2013
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Weese-Mayer DE et al.
Pediatric Research, 2004
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.
Weese-Mayer DE et al.
American Journal of Medical Genetics. Part A, 2003
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