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A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases.
Arthritis Rheum;
62(4): 1158-66, 2010 Apr.
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| MEDLINE | ID: mdl-20131270
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