Matches in Nanopublications for { ?s ?p "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1316486.RAKhxsNlHkMiWcXu3lwMabvmEixFOWOjrXCpTMWgcUdY0130_assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316486.RAKhxsNlHkMiWcXu3lwMabvmEixFOWOjrXCpTMWgcUdY0130_provenance.
- NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316489.RA1geL-wGlJ-oy6mynWXel93H7bcxr69r72K3J2FIGQSA130_provenance.