Matches in Nanopublications for { ?s ?p "[Leigh syndrome (LS) associated with cytochrome c oxidase (COX) deficiency is an autosomal recessive neurodegenerative disorder caused by mutations in SURF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_assertion description "[Leigh syndrome (LS) associated with cytochrome c oxidase (COX) deficiency is an autosomal recessive neurodegenerative disorder caused by mutations in SURF1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187473.RAm07Kftgne2gNNanvGtgl-8H_yAUA4eS_lT9OK8LmLfQ130_provenance.