Matches in Nanopublications for { ?s ?p "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442841.RASyZ9MM6IgUgo1wJWNU6u1WibgmLsZnS3NJYiNuhqv6Q130_provenance.
- assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP667988.RAQj-rvd5I-w83bJ4i0HN6o-DH01_iyUCFJzwHrLHE0pQ130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667988.RAQj-rvd5I-w83bJ4i0HN6o-DH01_iyUCFJzwHrLHE0pQ130_provenance.
- NP662221.RAtygDxjFPy9rnNTFs4CikjHPQqcGWc0h7RSReBr_dmcQ130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662221.RAtygDxjFPy9rnNTFs4CikjHPQqcGWc0h7RSReBr_dmcQ130_provenance.
- NP667987.RAuCkGMgn18w0DjwMDp3XvA1-XiUMjpWW6BZ0wSRrwowM130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667987.RAuCkGMgn18w0DjwMDp3XvA1-XiUMjpWW6BZ0wSRrwowM130_provenance.
- NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632434.RAIm6VMBN-CIel9rUKvwrbqePD8otIgspbb-Jr0MsLuGs130_provenance.
- NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_assertion description "[Charcot-Marie-Tooth type 1A (CMT1A) is an autosomal dominant polyneuropathy due to a 1.5 Mb tandem duplication in chromosome 17p11.2, containing the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667989.RA9FjvUoZ9Oq6mxidC5Qeh0hHLhHCeGULxuive71TpZ9g130_provenance.