Matches in Nanopublications for { ?s ?p "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance.
- NP568744.RAJ3RedctgoPQxFaRgodrWEoqP7ZWlgqLha2YD2JQ6sw8130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568744.RAJ3RedctgoPQxFaRgodrWEoqP7ZWlgqLha2YD2JQ6sw8130_provenance.
- NP375773.RADDmY8Gugf8zghIa2G4XEa_AwkYfjgrQENQBNLrXJrVc130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375773.RADDmY8Gugf8zghIa2G4XEa_AwkYfjgrQENQBNLrXJrVc130_provenance.
- NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977215.RACX0MqmC7yoO2UNE5x7M2gO_R482ehDNmnUFaYLLGtoA130_provenance.
- NP248433.RA4YyRwiVlkUQ37Ek-e-X9CzKTpvNldQZvLmhA6nmAPpE130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248433.RA4YyRwiVlkUQ37Ek-e-X9CzKTpvNldQZvLmhA6nmAPpE130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.