1. A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family. (5th July 2016) Authors: Shah, K.; Nasir, A.; Irfanullah, ; Shahzad, S.; Khan, S.; Ahmad, W. Journal: Clinical and experimental dermatology Issue: Volume 41:Number 6(2016) Page Start: 675 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗