Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP613156.RADqJCye3ynnEhW3azy323YKeODC1FAVy-dGjxhfGL8pI130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP613156.RADqJCye3ynnEhW3azy323YKeODC1FAVy-dGjxhfGL8pI130_provenance.
• NP899086.RAj8VTWhk67AnE6E4GK5fJ2GpPpMhK8mlSldk8kSj_rPM130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899086.RAj8VTWhk67AnE6E4GK5fJ2GpPpMhK8mlSldk8kSj_rPM130_provenance.
• NP371224.RA_ofRv59e9yVdk0vr6I7Y5CxfsjT4CXV9S0xiONEUwUY130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371224.RA_ofRv59e9yVdk0vr6I7Y5CxfsjT4CXV9S0xiONEUwUY130_provenance.
• NP323492.RAqVbkuyasdsNVdAkbiinJfpKC8_gCdcZUud1RZF__iAA130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323492.RAqVbkuyasdsNVdAkbiinJfpKC8_gCdcZUud1RZF__iAA130_provenance.
• NP683627.RApkz5fgWXdlzy77Z0a95vnvgSxlWPkRTZwuoxKywdN9E130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683627.RApkz5fgWXdlzy77Z0a95vnvgSxlWPkRTZwuoxKywdN9E130_provenance.
• NP874381.RAnG-bt6lMbDLpfL1S5T8OCn4hVWust6fKZpzZZ5A_D5o130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874381.RAnG-bt6lMbDLpfL1S5T8OCn4hVWust6fKZpzZZ5A_D5o130_provenance.
• NP598768.RAvxi2mKt9NBb-cDwo6tft3sg1_CWyo3YMF_J_m-WOHYs130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598768.RAvxi2mKt9NBb-cDwo6tft3sg1_CWyo3YMF_J_m-WOHYs130_provenance.
• NP844671.RAlK1eed9Q8Ku0W6d0j0GNaDIBNRhpBRWa70YT3xi0tec130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844671.RAlK1eed9Q8Ku0W6d0j0GNaDIBNRhpBRWa70YT3xi0tec130_provenance.
• NP486331.RAWYC7gW5hrJcau1XjHd4Vy-hZkdSMKx_PubSpVYZAs84130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486331.RAWYC7gW5hrJcau1XjHd4Vy-hZkdSMKx_PubSpVYZAs84130_provenance.
• NP912655.RAli8IbY0zCvTmVdvsDOMMoL6iyoC347zsP0xm8kvArW0130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912655.RAli8IbY0zCvTmVdvsDOMMoL6iyoC347zsP0xm8kvArW0130_provenance.
• NP192769.RAwWrSSlmrM43dTT81CxWdN7lNA13ulcOVSPAb9mwvrpM130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192769.RAwWrSSlmrM43dTT81CxWdN7lNA13ulcOVSPAb9mwvrpM130_provenance.
• NP612712.RA4DDQ0lfyTeNqc243-nILZok1VIC3ZRhlPfCgtpleSh0130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612712.RA4DDQ0lfyTeNqc243-nILZok1VIC3ZRhlPfCgtpleSh0130_provenance.
• NP778371.RA4-kwyHiHcekder3409jMfnR4tdrbIZZgnYiiZKbNG_8130_assertion description "[We describe a heterozygous dominant mutation (c.1352G-->A/p.G451E) in POLG2, the gene encoding the p55 accessory subunit of pol gamma , that causes progressive external ophthalmoplegia with multiple mtDNA deletions and cytochrome c oxidase (COX)-deficient muscle fibers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778371.RA4-kwyHiHcekder3409jMfnR4tdrbIZZgnYiiZKbNG_8130_provenance.