Matches in Nanopublications for { ?s ?p "[Using the Hereditary Hearing Loss arrayed primer extension (APEX) array, which contains 198 mutations across 8 hearing loss-associated genes (GJB2, GJB6, GJB3, GJA1, SLC26A4, SLC26A5, 12S-rRNA, and tRNA Ser), we compared the frequency of sequence variants in 94 individuals with early presbycusis to 50 unaffected controls and aimed to identify possible genetic contributors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_assertion description "[Using the Hereditary Hearing Loss arrayed primer extension (APEX) array, which contains 198 mutations across 8 hearing loss-associated genes (GJB2, GJB6, GJB3, GJA1, SLC26A4, SLC26A5, 12S-rRNA, and tRNA Ser), we compared the frequency of sequence variants in 94 individuals with early presbycusis to 50 unaffected controls and aimed to identify possible genetic contributors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650286.RAgdy0BwM8blvgQTF-8y6C9nKm22dX3LLGbqOaLytaF8M130_provenance.