Matches in Nanopublications for { ?s ?p "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.
- assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP280245.RAvhDWXemsZIjQDPMJihr-Qd-Ty-I7q4FpgbgWggzlJ3I130_assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280245.RAvhDWXemsZIjQDPMJihr-Qd-Ty-I7q4FpgbgWggzlJ3I130_provenance.
- NP280244.RA6DJ_R2e-DKCxEolXb6f5aKMVPbS3iSfaeAZoAA_F75E130_assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280244.RA6DJ_R2e-DKCxEolXb6f5aKMVPbS3iSfaeAZoAA_F75E130_provenance.