Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.

Krunic, Aleksandar L

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

Publication Type: Case Reports; Journal Article

1525-1470

10.1111/pde.12092 doi


Base Sequence
Codon, Nonsense
Consanguinity
Cystatin A--genetics
Dermatitis, Exfoliative--genetics
Family Health
Female
Homozygote
Humans
Male
Pedigree
Pigmentation Disorders--genetics
Skin Diseases--congenital