A novel homozygous mutation disrupting the initiation codon...

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.
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Volume:
41
Language:
english
Journal:
Clinical and Experimental Dermatology
DOI:
10.1111/ced.12864
Date:
August, 2016
File:
PDF, 547 KB
english, 2016
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