Cirillo, G <br/><br/>
Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysis.  [electronic resource] 

 -  The British journal of dermatology  Dec 2012 
 - 1393-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2133.2012.11060.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenocorticotropic Hormone--deficiency<br/>Adult<br/>Child, Preschool<br/>Codon, Nonsense--genetics<br/>Hair--chemistry<br/>Hair Color--genetics<br/>Homozygote<br/>Humans<br/>Hypoglycemia--drug therapy<br/>Male<br/>Melanins--analysis<br/>Nonsense Mediated mRNA Decay--genetics<br/>Obesity--genetics<br/>Pedigree<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Pro-Opiomelanocortin--genetics<br/>Young Adult