Matches in Nanopublications for { ?s ?p "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP826373.RAN1MVXHI0dNPcM3GQOprEB-Nfn4MvvbLdl1Fwqr6uS7w130_provenance.
- assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1392846.RA8OHCV2M1O8ZbBtWZmut3Cxd6s41TCghiX3fvNStwKOo130_provenance.
- NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1392847.RAFLK7QTHb9JreHoYnWNHxFNdr6OS6bBzreOGEcOi1kE8130_provenance.
- NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_assertion description "[X linked Charcot-Marie-Tooth disease (CMTX) is a hereditary motor and sensory neuropathy caused by mutations in the connexin 32 gene (Cx32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP426085.RApAnv5bFpKf_AlVZtfNvWyDtAAa6e-kMdQms4hF6-NhU130_provenance.