Matches in Nanopublications for { ?s ?p "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP848348.RAzVQvNrlLoe9SzU6tuSG75JvQueJ3OGxzIsbJEh-x028130_assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP848348.RAzVQvNrlLoe9SzU6tuSG75JvQueJ3OGxzIsbJEh-x028130_provenance.
- NP411501.RAVhyR-VSchAbDvsq_gh7SN1wYLvtgwb-cIbB9gFL66Hs130_assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP411501.RAVhyR-VSchAbDvsq_gh7SN1wYLvtgwb-cIbB9gFL66Hs130_provenance.
- assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346155.RA3WIuHnpUsgy4ml9mrJgRD3hf8PqPHtlNhSddg0JGoKc130_provenance.
- NP346157.RAeXB3oSuV5bA_-PN5G6hGVeoHA4pefkBExbRG63FXAA0130_assertion description "[Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346157.RAeXB3oSuV5bA_-PN5G6hGVeoHA4pefkBExbRG63FXAA0130_provenance.