Matches in Nanopublications for { ?s ?p "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP203666.RA1w29167lyYtrzqYYaZ8pMjYV0EOQsYc4fsGHeE0bvVU130_assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203666.RA1w29167lyYtrzqYYaZ8pMjYV0EOQsYc4fsGHeE0bvVU130_provenance.
- NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1333461.RAydSEOhoCJ8sX0TjS7FE8_SDWvmekFkokrYaeMBUg35A130_provenance.
- assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_assertion description "[The genetic data presents two alternative molecular mechanisms involving the PMP22 gene that result in the same clinical and electrophysiologic phenotype of CMT1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1333463.RALuy-FQvnJxIp4nfukn5JbkEU250jhvovQIXd5tsoiCw130_provenance.