Matches in Nanopublications for { ?s ?p "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP931419.RAkphIGk5Z6Dco_LTZKpX9tk6CxHEIVGgOgIXUrPBSLOw130_assertion description "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931419.RAkphIGk5Z6Dco_LTZKpX9tk6CxHEIVGgOgIXUrPBSLOw130_provenance.
- NP595592.RAYIUXlIFxoImAK1r61nHxsUCiDJ_iVQU2VTeCEtRHbfc130_assertion description "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595592.RAYIUXlIFxoImAK1r61nHxsUCiDJ_iVQU2VTeCEtRHbfc130_provenance.
- NP253272.RAFc3PPL348hJFT0arxpoVjg8djRVfrXtZVeuOySaBIiE130_assertion description "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253272.RAFc3PPL348hJFT0arxpoVjg8djRVfrXtZVeuOySaBIiE130_provenance.
- NP908080.RAFT-8_pOC2U_HgPNcUOTurSUaV_GIANsdzdIqgW3dCt8130_assertion description "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908080.RAFT-8_pOC2U_HgPNcUOTurSUaV_GIANsdzdIqgW3dCt8130_provenance.
- NP735505.RAK-tEliitZnPfSIjbwVmPADtcWNqZpg26waRlierMJjY130_assertion description "[PTC mutations in both alleles generally cause the most severe, mutilating Hallopeau-Siemens (HS) variant of RDEB, whereas none of the PTC mutations resulted in severe phenotypes consistent with the HS subtype when coupled with p.Glu2857X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735505.RAK-tEliitZnPfSIjbwVmPADtcWNqZpg26waRlierMJjY130_provenance.