Matches in Nanopublications for { ?s ?p "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353197.RAL3GOXAWPZRAwOBD9FYSRjiHXLMf2U4FupkjbE87ojH4130_provenance.