Genetic risk factors are also likely to be significant, with whole-exome sequencing identifying PIMS-associated mutations in the DOCK8 intracellular signalling proteins, cytochrome b-245 subunits, and X-linked inhibitors of apoptosis [ 70 ].
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Genetic risk factors are also likely to be significant, with whole-exome sequencing identifying PIMS-associated mutations in the DOCK8 intracellular signalling proteins, cytochrome b-245 subunits, and X-linked inhibitors of apoptosis [ 70 ].