Matches in Nanopublications for { ?s ?p "[We report a novel truncating mutation in DFNB31 associated with severe rod-cone dystrophy and varying degrees of hearing impairment in a consanguineous family of Portuguese origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP852662.RA0GlXLyw5x5hGn4Zk06QtDjkTlR8b_uPikonJmLj1iqM130_assertion description "[We report a novel truncating mutation in DFNB31 associated with severe rod-cone dystrophy and varying degrees of hearing impairment in a consanguineous family of Portuguese origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852662.RA0GlXLyw5x5hGn4Zk06QtDjkTlR8b_uPikonJmLj1iqM130_provenance.
- assertion description "[We report a novel truncating mutation in DFNB31 associated with severe rod-cone dystrophy and varying degrees of hearing impairment in a consanguineous family of Portuguese origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP907958.RAQbScRaPgdqVhsefYdD0-FSF3reZpuBXTG29fBSY9q5o130_assertion description "[We report a novel truncating mutation in DFNB31 associated with severe rod-cone dystrophy and varying degrees of hearing impairment in a consanguineous family of Portuguese origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907958.RAQbScRaPgdqVhsefYdD0-FSF3reZpuBXTG29fBSY9q5o130_provenance.
- NP879378.RAAh0UcK846vSUZYz4FXpq13Mif5QtS1h0iAPCcxZl_MA130_assertion description "[We report a novel truncating mutation in DFNB31 associated with severe rod-cone dystrophy and varying degrees of hearing impairment in a consanguineous family of Portuguese origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879378.RAAh0UcK846vSUZYz4FXpq13Mif5QtS1h0iAPCcxZl_MA130_provenance.