Betlloch, Isabel <br/><br/>
Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.  [electronic resource] 

 -  Pediatric dermatology   
 - 489-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1525-1470 
<br/><br/><label>Standard No.: </label>10.1111/j.1525-1470.2009.00969.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenine<br/>Base Sequence<br/>DNA<br/>Female<br/>Guanine<br/>Heterozygote<br/>Humans<br/>Hyperkeratosis, Epidermolytic--complications<br/>Infant, Newborn<br/>Keratin-10--genetics<br/>Point Mutation<br/>Protein Structure, Tertiary<br/>Staphylococcal Scalded Skin Syndrome--complications