Matches in Nanopublications for { ?s ?p "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316688.RAlBBPP9HwzPLVEcQvoxl3O1_kdaagkgYbdZg6dOn2xQA130_provenance.
- NP254912.RAG5YTQp1JXj82z8BVlP8b9en7Nq2ELyFaicSgym9MElY130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254912.RAG5YTQp1JXj82z8BVlP8b9en7Nq2ELyFaicSgym9MElY130_provenance.
- NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810923.RASWOZuXtA_1y1o-AtIrPape6hWcYxD1ILdWqA7kFlAks130_provenance.
- assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810940.RAtOMV3Ehd6vBhTLpyHktvFSCSPcAliO4a__CwWzdyuFk130_provenance.
- NP678165.RAvFdhZ8MTn2HKSsIJ-AOSTC5V7hY3Y3x7ZNMU6Ds8a6g130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678165.RAvFdhZ8MTn2HKSsIJ-AOSTC5V7hY3Y3x7ZNMU6Ds8a6g130_provenance.
- NP678166.RAyK7YTS_vdT4idSQYrEvM_aIUexZpawXRMrkrXYY3Vxc130_assertion description "[Myoclonus-dystonia (M-D) is an autosomal dominantly inherited movement disorder with myoclonic jerks and dystonic contractions most frequently due to a mutation in the epsilon-sarcoglycan (SGCE, DYT11) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678166.RAyK7YTS_vdT4idSQYrEvM_aIUexZpawXRMrkrXYY3Vxc130_provenance.