Matches in Nanopublications for { ?s ?p "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP175064.RASr2oYjez53vR8OumOcLwEjJm8y5aMElmtB08kM7SEkM130_assertion description "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175064.RASr2oYjez53vR8OumOcLwEjJm8y5aMElmtB08kM7SEkM130_provenance.
- NP650733.RAnryctdBNy09Q0NRBlNXbQT2VyvBccTuRgUPii7vMpkA130_assertion description "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650733.RAnryctdBNy09Q0NRBlNXbQT2VyvBccTuRgUPii7vMpkA130_provenance.
- NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_assertion description "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576665.RA1ay9YImeObNBxajWEqVOuT41j9GKLi1YqbmEd7wvWFc130_provenance.
- NP470152.RAFcXyO8up2WpG-UxI2fYLPOGtoKl5h1Adbh7KCVLdJ1k130_assertion description "[We analyzed 98 Japanese families with autosomal dominant SCAs, for whom CAG repeat expansions of the SCA1, SCA2, Machado-Joseph disease/SCA3, and dentatorubral-pallidoluysian atrophy genes were excluded, and 5 apparently sporadic cases of cortical cerebellar atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470152.RAFcXyO8up2WpG-UxI2fYLPOGtoKl5h1Adbh7KCVLdJ1k130_provenance.