Matches in Nanopublications for { ?s ?p "[Perforin gene (PRF1) mutations have been reported in 20-30% of patients with familial hemophagocytic lymphohistiocytosis (FHL), an immune disorder of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP639874.RApgslxLWavECDpCKvVpGfEPchE-qAjhPZ9_3CWCaWp3k130_assertion description "[Perforin gene (PRF1) mutations have been reported in 20-30% of patients with familial hemophagocytic lymphohistiocytosis (FHL), an immune disorder of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639874.RApgslxLWavECDpCKvVpGfEPchE-qAjhPZ9_3CWCaWp3k130_provenance.
- NP621670.RArxHhrdJ7oLnGxjrY1Z2HOP1BSfwFEdLBfzSIpDn8rME130_assertion description "[Perforin gene (PRF1) mutations have been reported in 20-30% of patients with familial hemophagocytic lymphohistiocytosis (FHL), an immune disorder of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621670.RArxHhrdJ7oLnGxjrY1Z2HOP1BSfwFEdLBfzSIpDn8rME130_provenance.