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497707
497707
http://dx.doi.org/10.1086/497707
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome
P356
Q24538571-A3EE75B0-1E21-4C85-9E9B-A064564D3BAD
P356
497707
http://dx.doi.org/10.1086/497707