Matches in Nanopublications for { ?s ?p "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477649.RAafLmaOoz3pqt7QjYrYpLIUNiJeKt2N_RyJ6rgl9uasM130_provenance.
- NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908959.RAaVaJLpxzCGg2no4sUczIrEMEcwBpS9C4VbceXOYX760130_provenance.
- NP799438.RAp37gzzvxAcxiKxY0armdcsIw1eMg4wWCQpTliY2uKnI130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799438.RAp37gzzvxAcxiKxY0armdcsIw1eMg4wWCQpTliY2uKnI130_provenance.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.