Matches in Nanopublications for { ?s ?p "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP522063.RABAW_2afj9g9JL2Y6YGEa4x0DWXCjmB8M0liIV2wOEoE130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522063.RABAW_2afj9g9JL2Y6YGEa4x0DWXCjmB8M0liIV2wOEoE130_provenance.
- NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507329.RA-885aed75eHlwX35-ah04kQMJpXEQNw31ROTPu6YznA130_provenance.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.
- NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651914.RAJz-Xt7AE35HyxWqwnNgCZyCuwLgTeyoq5AxUZ9IOVPU130_provenance.