Matches in Nanopublications for { ?s ?p "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP436902.RAAZrmGViqFsjpfZIBvT6e9_R3hQmX4D48u39kL0EhCbI130_assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436902.RAAZrmGViqFsjpfZIBvT6e9_R3hQmX4D48u39kL0EhCbI130_provenance.
- NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616284.RA4XT-FmAAhh3czCsJ7DEA9uGHxMCzxcpYCWeImQ_XZ8o130_provenance.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.
- assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.