Matches in Nanopublications for { ?s ?p "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836796.RAbGLHPQq_3Ocn8kfopjpxEmSHQW3pqb5F4IhNQWMliTY130_provenance.
- NP586859.RAHxgaQ6W2pa-t6pg4Xq3OV17Doi4EHvMiQMNV91CGSWg130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586859.RAHxgaQ6W2pa-t6pg4Xq3OV17Doi4EHvMiQMNV91CGSWg130_provenance.
- NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867654.RAUsc2N_PzcDGJ_3my0cp5E-U4wXZ77YJG9lznfmBe_CI130_provenance.
- NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867647.RAik7vSXgW3Y82xhH4kRS0Kd3lquV2_w5-0Z_7obh4t-I130_provenance.
- NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_assertion description "[LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836872.RAJj4itIGDFBVsyII6SBH-WI9lJAJHrnyH4v1F2IzuY_s130_provenance.