Matches in Nanopublications for { ?s ?p "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP120782.RAgyngovD7uREr4uOYiFk4L_BOVXOGQ1tLT82sN_9aVkA130_assertion description "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120782.RAgyngovD7uREr4uOYiFk4L_BOVXOGQ1tLT82sN_9aVkA130_provenance.
- assertion description "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_assertion description "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183973.RAADs8dKNHIsKZ1TohqDTLojX_OlDZafvWKbGUEYkWylg130_provenance.
- NP243165.RAw2xZAY7EUMjSMjMQYl8oaBBX1QEMUPsVFDC9m_T36qs130_assertion description "[Mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243165.RAw2xZAY7EUMjSMjMQYl8oaBBX1QEMUPsVFDC9m_T36qs130_provenance.