Matches in Nanopublications for { ?s ?p "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP374043.RATciMQmvE-jzNgP2zlg1sgGWCqA83bJD7GCVt6QOYGeE130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374043.RATciMQmvE-jzNgP2zlg1sgGWCqA83bJD7GCVt6QOYGeE130_provenance.
- NP584181.RAYshMFlAILpzbzyJvXCg77WwAYo7cIJwroGbNUmQsImg130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584181.RAYshMFlAILpzbzyJvXCg77WwAYo7cIJwroGbNUmQsImg130_provenance.
- assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277154.RAeCxt-AX38BB_vQJUsmCTKw9V3U_GNeyCndh1KtPq21U130_provenance.
- NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584172.RAi31vdGn5UG3Oj-NV79D76LZ5PdtgTrXXkajsK9LXDU0130_provenance.
- NP277152.RALJ26GEyzeQ-QGT8Ft9Fl3f3GeLO2vL8R5sFyoQos9sY130_assertion description "[The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and dominant nonsyndromic hearing loss (DFNB2 and DFNA11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277152.RALJ26GEyzeQ-QGT8Ft9Fl3f3GeLO2vL8R5sFyoQos9sY130_provenance.