Matches in Nanopublications for { ?s ?p "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 9 of
9
with 100 items per page.
- NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895476.RAhzS7XCGXMODaag3KbJ0fPnampfi9AVlWfWr0zTD3Wss130_provenance.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.
- NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583290.RAeBUGUCOxZUXZYiqqThTBes0Wf4w3xBaZW54jLe8CpTY130_provenance.
- assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709219.RAJyiCM8GCbCxf15ufk2JOP7lYcSjwDMy4OpxZRF0Vifs130_provenance.
- NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584056.RA28_6JTBVJo1ydtiyViHw16lQt1SAfIlpeviF1WJofW0130_provenance.
- NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390498.RAJGQA0WT2kLwmRh_RNQVN62sacq_GU9R3z0Dn8qIXxts130_provenance.
- NP390499.RAFhPFVxN9nNIQv1aILXekJHKhwikqNnQB1nIKhVHP6Yw130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390499.RAFhPFVxN9nNIQv1aILXekJHKhwikqNnQB1nIKhVHP6Yw130_provenance.