Matches in Nanopublications for { ?s ?p "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP288799.RAQVU8Vpk4e7MtElAZAA_HhlHifzkt0qJbvFNVSETEV2g130_assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP288799.RAQVU8Vpk4e7MtElAZAA_HhlHifzkt0qJbvFNVSETEV2g130_provenance.
- NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931389.RAbhQZxpezMTlIoygk-6Eb6w7bnAuWHCw3sBOX4CokI34130_provenance.
- NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720639.RA-XHWAAcndXDo6u1k2unSHIvmF8JUPEuu14XbdRbJIfs130_provenance.
- NP767492.RA35fiLqiehS6x4VypD-FTd73WZ70SmwMqVOC6knEDxbY130_assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767492.RA35fiLqiehS6x4VypD-FTd73WZ70SmwMqVOC6knEDxbY130_provenance.
- assertion description "[Mutations in the nuclear SURF-1 gene lead directly to cytochrome-c oxidase deficiency, the most common respiratory chain defect in Leigh syndrome, a neurodegenerative mitochondrial disease involving the deep gray matter and brain stem.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.