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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- NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_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." NP162579.RAml7oCtTyHHYQZlDMuJBLPVlb2583OgqgyhIAL2IfLQQ130_provenance.