Matches in Nanopublications for { ?s ?p "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP431742.RA_ZaMar-1EYyCIfWEX060L_nuuDEn6JzjCa_-X5Js60I130_assertion description "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431742.RA_ZaMar-1EYyCIfWEX060L_nuuDEn6JzjCa_-X5Js60I130_provenance.
- NP3256.RAskkViLNIqje0v5cQizkrgHeqKLQwwk47A2nLgqbIzn0130_assertion description "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3256.RAskkViLNIqje0v5cQizkrgHeqKLQwwk47A2nLgqbIzn0130_provenance.
- NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_assertion description "[By phenotypic analysis of affected relatives and carriers of the same ELA2 mutations, we showed that the expression of neutropenia in CN and SCN may be either homogeneous or variable according to the type of mutations, suggesting different pathogenetic mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431749.RAMXhGwiiUSADQJ_iI99RWa2dXyDgMu89SP9XD889Ej9o130_provenance.