Matches in Nanopublications for { ?s ?p "[Three novel CTSC missense mutations found in 21 Papillon-Lefevre syndrome families, and a complete loss of CTSC function appears to be necessary for the manifestation of this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP121885.RAl6lYmSv55soJqpGQXmJS8eZBWPKF65hGdgUjgOIvlA4130_assertion description "[Three novel CTSC missense mutations found in 21 Papillon-Lefevre syndrome families, and a complete loss of CTSC function appears to be necessary for the manifestation of this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121885.RAl6lYmSv55soJqpGQXmJS8eZBWPKF65hGdgUjgOIvlA4130_provenance.
- assertion description "[Three novel CTSC missense mutations found in 21 Papillon-Lefevre syndrome families, and a complete loss of CTSC function appears to be necessary for the manifestation of this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP185074.RAsttpymKnUwSclFlMJKWoZIPoP5FphOJaeN-xOPu-s50130_assertion description "[Three novel CTSC missense mutations found in 21 Papillon-Lefevre syndrome families, and a complete loss of CTSC function appears to be necessary for the manifestation of this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185074.RAsttpymKnUwSclFlMJKWoZIPoP5FphOJaeN-xOPu-s50130_provenance.
- NP203634.RAvVmGU2B9C4Kj_5wnem_PbcQ_HawrAXrKb6UNqtTnpBA130_assertion description "[Three novel CTSC missense mutations found in 21 Papillon-Lefevre syndrome families, and a complete loss of CTSC function appears to be necessary for the manifestation of this phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203634.RAvVmGU2B9C4Kj_5wnem_PbcQ_HawrAXrKb6UNqtTnpBA130_provenance.