Matches in Nanopublications for { ?s ?p "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion description "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion description "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.