Matches in Nanopublications for { ?s ?p "[These results demonstrate that the ATXN2 CAG expansion is the sole causative mutation responsible for SCA2-P, and that genetic modifiers may not be the major cause of the phenotypic diversity of SCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[These results demonstrate that the ATXN2 CAG expansion is the sole causative mutation responsible for SCA2-P, and that genetic modifiers may not be the major cause of the phenotypic diversity of SCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_assertion description "[These results demonstrate that the ATXN2 CAG expansion is the sole causative mutation responsible for SCA2-P, and that genetic modifiers may not be the major cause of the phenotypic diversity of SCA2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216880.RA4dWAB7LfsclfnNJdL7jPmx4xJ02hZOKdaw6FuuZl1Qw130_provenance.