Matches in Nanopublications for { ?s ?p "[This observation identifies ACO2 as the second gene responsible for non-syndromic autosomal recessive optic neuropathies and provides evidence for a genetic overlap between isolated and syndromic forms, giving further support to the view that optic atrophy is a hallmark of defective mitochondrial energy supply.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[This observation identifies ACO2 as the second gene responsible for non-syndromic autosomal recessive optic neuropathies and provides evidence for a genetic overlap between isolated and syndromic forms, giving further support to the view that optic atrophy is a hallmark of defective mitochondrial energy supply.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[This observation identifies ACO2 as the second gene responsible for non-syndromic autosomal recessive optic neuropathies and provides evidence for a genetic overlap between isolated and syndromic forms, giving further support to the view that optic atrophy is a hallmark of defective mitochondrial energy supply.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1233338.RAB3Ca6f_d0PsPV1JFHznl-WqNPoVHHz6LPNpX0WZ66xo130_assertion description "[This observation identifies ACO2 as the second gene responsible for non-syndromic autosomal recessive optic neuropathies and provides evidence for a genetic overlap between isolated and syndromic forms, giving further support to the view that optic atrophy is a hallmark of defective mitochondrial energy supply.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1233338.RAB3Ca6f_d0PsPV1JFHznl-WqNPoVHHz6LPNpX0WZ66xo130_provenance.
- NP1233339.RAt0XhD4czH2IYU-0RxfXhFr20VE6wlIrD8P8ysdACUtE130_assertion description "[This observation identifies ACO2 as the second gene responsible for non-syndromic autosomal recessive optic neuropathies and provides evidence for a genetic overlap between isolated and syndromic forms, giving further support to the view that optic atrophy is a hallmark of defective mitochondrial energy supply.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1233339.RAt0XhD4czH2IYU-0RxfXhFr20VE6wlIrD8P8ysdACUtE130_provenance.