Trochet, Delphine <br/><br/>
Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).  [electronic resource] 

 -  Human mutation  May 2008 
 - 770 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.20727  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alanine--genetics<br/>Alleles<br/>Female<br/>Genes, Dominant<br/>Homeodomain Proteins--genetics<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Pedigree<br/>Sleep Apnea, Central--genetics<br/>Transcription Factors--genetics