Kwon, Kyoung-Ah <br/><br/>
A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate.  [electronic resource] 

 -  Journal of Korean medical science  Aug 2010 
 - 1237-40 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1598-6357 
<br/><br/><label>Standard No.: </label>10.3346/jkms.2010.25.8.1237  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Asian People--genetics<br/>Genotype<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Hypoventilation--congenital<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Peptides--genetics<br/>Republic of Korea<br/>Sequence Analysis, DNA<br/>Transcription Factors--genetics<br/>Ventilators, Mechanical