Research Letter
A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B
Funding sources: This work was supported by funding from the Samuel Hardgrave Harlequin Ichthyosis Research Trust (SHHiRT) and the Ichthyosis Support Group (ISG) awarded to D.P.K.
Conflicts of interest: none declared.
