Matches in Nanopublications for { ?s ?p "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066786.RAXqz3eofJV3YVABtgE9xjfc9uX_e7r_6WWa3YI4dAbyk130_provenance.
- NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584143.RAtSE_OiVoK7vUvhYcncdgCwkpmqpN1upgSemA1d33Xpc130_provenance.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.
- NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7434.RAEVzQdzylF8fxBcDVRvkR1ofGPNKdINWMqgynb_5QLTQ130_provenance.
- NP1066787.RANcPtDJnFJfYbWZ-qoMI-Z_4e7a6MJp4Ee9xyjl1b4dQ130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066787.RANcPtDJnFJfYbWZ-qoMI-Z_4e7a6MJp4Ee9xyjl1b4dQ130_provenance.