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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- NP849094.RA8yiOvimftLWuN3YEMWciF02DiWrTkpu-y1jxlIHgZ3A130_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." NP849094.RA8yiOvimftLWuN3YEMWciF02DiWrTkpu-y1jxlIHgZ3A130_provenance.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_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." NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.
- NP615036.RAG5xIZRVe_qZg6sc3cd-4Ocr_amPze9WrSmbQFX2xEb0130_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." NP615036.RAG5xIZRVe_qZg6sc3cd-4Ocr_amPze9WrSmbQFX2xEb0130_provenance.
- NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_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." NP6415.RAhO5YbMAWEECy0o5CWrBx9xhpPgM7FsKEHjezjHkE8pQ130_provenance.
- NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_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." NP615085.RAhggoJSWTLaNFsgFSiCnCQEQBTtLeXqCh4TvKEe7iT74130_provenance.