Matches in Nanopublications for { ?s ?p "[The archetypal NARP syndrome is almost exclusively associated with the m.8993T>C/G mutation in the sixth subunit of the mitochondrial ATP synthase, whereas other mutations in the MT-ATP6 gene primarily associate with Leigh syndrome or Leber's hereditary optic neuropathy (LHON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 3 of
3
with 100 items per page.
- NP685045.RAC9FNT3KkXsT5F5d-x2FZIhGFgMpcIfERgyOaQGxSLSQ130_assertion description "[The archetypal NARP syndrome is almost exclusively associated with the m.8993T>C/G mutation in the sixth subunit of the mitochondrial ATP synthase, whereas other mutations in the MT-ATP6 gene primarily associate with Leigh syndrome or Leber's hereditary optic neuropathy (LHON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP685045.RAC9FNT3KkXsT5F5d-x2FZIhGFgMpcIfERgyOaQGxSLSQ130_provenance.
- NP696807.RAAv582dVm3lu-yL-aHf49LDZtec2R2qF2WiY77R-z3hY130_assertion description "[The archetypal NARP syndrome is almost exclusively associated with the m.8993T>C/G mutation in the sixth subunit of the mitochondrial ATP synthase, whereas other mutations in the MT-ATP6 gene primarily associate with Leigh syndrome or Leber's hereditary optic neuropathy (LHON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696807.RAAv582dVm3lu-yL-aHf49LDZtec2R2qF2WiY77R-z3hY130_provenance.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion description "[The archetypal NARP syndrome is almost exclusively associated with the m.8993T>C/G mutation in the sixth subunit of the mitochondrial ATP synthase, whereas other mutations in the MT-ATP6 gene primarily associate with Leigh syndrome or Leber's hereditary optic neuropathy (LHON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.