Matches in Nanopublications for { ?s ?p "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP147665.RAr8_-ZAXBAlDmWDz4xfGB92X7Jh5OboT-qD_YB4eZHVM130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147665.RAr8_-ZAXBAlDmWDz4xfGB92X7Jh5OboT-qD_YB4eZHVM130_provenance.
- NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120772.RA3UKIwg4JkFWPdi6Jha6uMZeQxnHNk7lVz_c5j2tQXJY130_provenance.
- NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210797.RASXCwnK0EUsYJ5DN2ToE3a-eTHCwHzluAHJOi2ghi198130_provenance.
- assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183963.RAk_DLnKXJpKPD_Ru6GApzT_4qNLrh_qEB-qUaUQtseRw130_provenance.
- NP216202.RAmzxERchk6FHy27AnIKB_1RMowkI2j5AZRQQvi8SZetc130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216202.RAmzxERchk6FHy27AnIKB_1RMowkI2j5AZRQQvi8SZetc130_provenance.
- NP216205.RAj-HNP4Pc8Gec5h1bYaWFzOASrfdIAl5gKfNvSPWzI9s130_assertion description "[Missense mutations within a defined region are associated with dominant low-frequency hearing loss (DFNA6/14/38), while more severe mutations spanning WFS1 are found in Wolfram syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216205.RAj-HNP4Pc8Gec5h1bYaWFzOASrfdIAl5gKfNvSPWzI9s130_provenance.