Matches in Nanopublications for { ?s ?p "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (?0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (?0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (?0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (?0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.