Matches in Nanopublications for { ?s ?p "[The results underlined the importance of considering the complete DNA sequencing of the SLC26A4 gene for differential molecular diagnosis of deafness, especially in those patients affected by congenital, progressive and fluctuating mixed hearing loss with bilateral EVA.]. 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.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion description "[The results underlined the importance of considering the complete DNA sequencing of the SLC26A4 gene for differential molecular diagnosis of deafness, especially in those patients affected by congenital, progressive and fluctuating mixed hearing loss with bilateral EVA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.