Matches in Nanopublications for { ?s ?p "[Mutations in the SLC26A4 gene (7q22.3-7q31.1) are considered one of the most common causes of genetic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_assertion description "[Mutations in the SLC26A4 gene (7q22.3-7q31.1) are considered one of the most common causes of genetic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991629.RAkQPljUAQSnO3uzj_7xPoR48dzsQlqu2qthbvg0qN8is130_provenance.