Matches in Nanopublications for { ?s ?p "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.
- NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583641.RAqFrHsB2hmHhE7oK4X9q-5sizV3lltQLlU_W0_tukCJU130_provenance.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.
- assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530474.RA7U-YhwQkqbznp0gnZwc0tRKi77z0i1wzVsLqNOHm8Eo130_provenance.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.