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EXD.12262
EXD.12262
http://dx.doi.org/10.1111/EXD.12262
A new KRT16 mutation associated with a phenotype of pachyonychia congenita.
P356
Q54775852-01C9B3D0-25A3-4B4E-BC3D-630FC0E90CF3
P356
EXD.12262
http://dx.doi.org/10.1111/EXD.12262