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BJD.15308
BJD.15308
http://dx.doi.org/10.1111/BJD.15308
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function.
P356
Q52842500-4327F120-6F38-44B4-9E62-23D1FA8A259D
P356
BJD.15308
http://dx.doi.org/10.1111/BJD.15308