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Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency
Burbank, Allison J., Shah, Shaili N., Montgomery, Maureen, Peden, David, Tarrant, Teresa K., Weimer, Eric T.Volume:
27
Language:
english
Journal:
Pediatric Allergy and Immunology
DOI:
10.1111/pai.12451
Date:
February, 2016
File:
PDF, 243 KB
english, 2016