Krunic, Aleksandar L <br/><br/>
Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.  [electronic resource] 

 -  Pediatric dermatology   
 - e87-8 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/pde.12092  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Codon, Nonsense<br/>Consanguinity<br/>Cystatin A--genetics<br/>Dermatitis, Exfoliative--genetics<br/>Family Health<br/>Female<br/>Homozygote<br/>Humans<br/>Male<br/>Pedigree<br/>Pigmentation Disorders--genetics<br/>Skin Diseases--congenital