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PDE.12092
PDE.12092
http://dx.doi.org/10.1111/PDE.12092
Acral peeling skin syndrome resulting from a homozygous nonsense mutation in the CSTA gene encoding cystatin A.
P356
Q44909039-4098C94D-9073-4A59-8603-34C14341E478
P356
PDE.12092
http://dx.doi.org/10.1111/PDE.12092