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 (a1/40.5%) 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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- NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (a1/40.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815.RAiSW3ESlPnZu7u5I6W1NcjPFoSISrf7Vr3OdOUqZff8c130_provenance.