Matches in Nanopublications for { ?s ?p "[Based on the studies in mice, we screened DNA from human families segregating deafness and identified a mutation in LOXHD1, which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL).]. 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.
- NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_assertion description "[Based on the studies in mice, we screened DNA from human families segregating deafness and identified a mutation in LOXHD1, which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868381.RAxvdXwZsRu66D49_nc15VU7jWnKsDWtjpXkIcyPreDSw130_provenance.