Congenital central hypoventilation syndrome:PHOX2B genotype determines risk for sudden death-Reference-Cited by-同舟云学术

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Congenital central hypoventilation syndrome:PHOX2B genotype determines risk for sudden death

Published:2007 Issue:1 Volume:43 Page:77-86
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr. Pulmonol.

Author:

Gronli Jerome O.,Santucci Barbara A.,Leurgans Sue E.,Berry-Kravis Elizabeth M.,Weese-Mayer Debra E.

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Reference30 articles.

1. Pediatric Autonomic Disorders

2. Idiopathic Congenital Central Hypoventilation Syndrome

3. Facial Phenotype in Children and Young Adults with PHOX2B–Determined Congenital Central Hypoventilation Syndrome: Quantitative Pattern of Dysmorphology

4. Adult Identified with Congenital Central Hypoventilation Syndrome–Mutation inPHOX2bGene and Late-Onset CHS

5. PHOX2BMutation–confirmed Congenital Central Hypoventilation Syndrome

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