Congenital Central Hypoventilation Syndrome in Children
Author:
Publisher
Elsevier BV
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference57 articles.
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2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet.,2003
3. Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b;Weese-Mayer;Am J Med Genet A.,2003
4. PHOX2B germline and somatic mutations in late-onset central hypoventilation syndrome;Trochet;Am J Respir Crit Care Med.,2008
5. The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype;Trang;Chest.,2005
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