Matches in Nanopublications for { ?s ?p "[Mutations of the gap junction beta 2 (GJB2) gene coding for the protein connexin 26 account for up to 50% of nonsyndromic sensorineural hearing loss (NSHL), with specific mutations associated with distinct ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_assertion description "[Mutations of the gap junction beta 2 (GJB2) gene coding for the protein connexin 26 account for up to 50% of nonsyndromic sensorineural hearing loss (NSHL), with specific mutations associated with distinct ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642766.RAA9-fV1nezomUifYwV9WTM9R9GOu0GO_KaGb9QXYJX9Q130_provenance.
- NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_assertion description "[Mutations of the gap junction beta 2 (GJB2) gene coding for the protein connexin 26 account for up to 50% of nonsyndromic sensorineural hearing loss (NSHL), with specific mutations associated with distinct ethnic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743751.RA7J4Kf_0BbCGjYSAoYvAVo8SMhFbhV9S6eRnSx8Bm9YI130_provenance.