PHOX2BMutation–confirmed Congenital Central Hypoventilation Syndrome-Reference-Cited by-同舟云学术

PHOX2BMutation–confirmed Congenital Central Hypoventilation Syndrome

Published:2006-10-15 Issue:8 Volume:174 Page:923-927
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Antic Nick A.,Malow Beth A.,Lange Neale,McEvoy R. Doug,Olson Amy L.,Turkington Peter,Windisch Wolfram,Samuels Martin,Stevens Cathy A.,Berry-Kravis Elizabeth M.,Weese-Mayer Debra E.

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference12 articles.

1. Idiopathic Congenital Central Hypoventilation Syndrome

2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

3. Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

4. Molecular analysis of congenital central hypoventilation syndrome

5. PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

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