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Objective
To elucidate the genetic background of a patient with neonatal‐onset multisystem inflammatory disease (NOMID) with no NLRP3 mutation.
Methods
A Japanese male child diagnosed as having NOMID was studied. The patient did not have any NLRP3 mutation, even as low‐frequency mosaicism. We performed whole‐exome sequencing on the patient and his parents. Induced pluripotent stem cells (iPSCs)...
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