Matches in Nanopublications for { ?s ?p "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP704461.RAxchErQfRgGJXcDj3a9zFkm-rJDZlpo3GXC4pXoCebY0130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704461.RAxchErQfRgGJXcDj3a9zFkm-rJDZlpo3GXC4pXoCebY0130_provenance.
- NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446505.RADg6wuc6PkQuEAkjSr-uo4Zry5RdwCNY7NUOiJgo_TLg130_provenance.
- NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256090.RA88W6Q5H0L4C7QIOiixcKkv7ArYJ1aDUkoBPc6S7IgY0130_provenance.
- NP446504.RAF0CYIQYsy3VPDjdLs8n5DFAK5zDf9QQkdP-n0buA1qw130_assertion description "[We report a novel ATP1A2 mutation in a kindred with features that bridge the phenotypic spectrum between AHC and FHM syndromes, supporting a possible common pathogenesis in a subset of such cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446504.RAF0CYIQYsy3VPDjdLs8n5DFAK5zDf9QQkdP-n0buA1qw130_provenance.