Matches in Nanopublications for { ?s ?p "[In a Turkish family, we identified a novel point mutation in the XDH gene responsible for classical type I xanthinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_assertion description "[In a Turkish family, we identified a novel point mutation in the XDH gene responsible for classical type I xanthinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465203.RA03rU2OWYTMEq20tTqv4lk79pe25y8yThun73HxlYDUE130_provenance.