![](/img/cover-not-exists.png)
A novel homozygous mutation disrupting the initiation codon in the SLURP1 gene underlies mal de Meleda in a consanguineous family
Shah, K., Nasir, A., Irfanullah, , Shahzad, S., Khan, S., Ahmad, W.Volume:
41
Language:
english
Journal:
Clinical and Experimental Dermatology
DOI:
10.1111/ced.12864
Date:
August, 2016
File:
PDF, 547 KB
english, 2016