Matches in Nanopublications for { ?s ?p "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_assertion description "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583587.RAIJr3rh7I-cz6wt7Jxck1VE1F9PVHEsdKhE0wXCsw984130_provenance.
- NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_assertion description "[Thus, we tested the hypothesis that a mutation within MYH9 is responsible for the autosomal dominant inheritance of MTCP and hearing loss in the Ghent family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725929.RAFOKrj42pzs7Xp62Jxl2JqgcseTmV17zlGbokinLI6SE130_provenance.