Matches in Nanopublications for { ?s ?p "[The most common genetic cause of the inherited peripheral neuropathy Charcot-Marie-Tooth disease is the PMP22 duplication; otherwise, CNVs have been considered rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_assertion description "[The most common genetic cause of the inherited peripheral neuropathy Charcot-Marie-Tooth disease is the PMP22 duplication; otherwise, CNVs have been considered rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260756.RAs2fD_Qixe9_wWdqV4ps57vYVleAVZl5dpYhm1WFoERs130_provenance.
- NP1260757.RA0hx2IsvF3-aN6blsox92re3_Hled4No26cE9J4s6Py0130_assertion description "[The most common genetic cause of the inherited peripheral neuropathy Charcot-Marie-Tooth disease is the PMP22 duplication; otherwise, CNVs have been considered rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260757.RA0hx2IsvF3-aN6blsox92re3_Hled4No26cE9J4s6Py0130_provenance.