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Journal Abstract Search

188 related items for PubMed ID: 21478040

  • 21. Mitochondrial deoxyribonucleotide pools in deoxyguanosine kinase deficiency.
    Saada A.
    Mol Genet Metab; 2008 Nov; 95(3):169-73. PubMed ID: 18723380
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  • 22. Pathology teach and tell: neonatal hemochromatosis with massive hepatic necrosis.
    Goyal R, Pattari SK, Kakkar N, Radotra BD, Narang A.
    Fetal Pediatr Pathol; 2004 Nov; 23(5-6):345-50. PubMed ID: 16137172
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  • 23. Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.
    Elpeleg O, Mandel H, Saada A.
    J Mol Med (Berl); 2002 Jul; 80(7):389-96. PubMed ID: 12110944
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  • 25. Mitochondrial DNA depletion and dGK gene mutations.
    Salviati L, Sacconi S, Mancuso M, Otaegui D, Camaño P, Marina A, Rabinowitz S, Shiffman R, Thompson K, Wilson CM, Feigenbaum A, Naini AB, Hirano M, Bonilla E, DiMauro S, Vu TH.
    Ann Neurol; 2002 Sep; 52(3):311-7. PubMed ID: 12205643
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  • 26. [Neonatal hemochromatosis. Report of 3 autopsy cases].
    Rodríguez Velasco A, García GR, Tejeda Vega S, Sjordia Reyes GA, Ferman Cano F, Cantú Cuevas MA.
    Rev Invest Clin; 1999 Sep; 51(2):81-7. PubMed ID: 10410586
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  • 27. Mitochondrial deoxyguanosine kinase mutations and mitochondrial DNA depletion syndrome.
    Wang L, Eriksson S.
    FEBS Lett; 2003 Nov 20; 554(3):319-22. PubMed ID: 14623087
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  • 36. Neonatal hemochromatosis: diagnostic work-up based on a series of 56 cases of fetal death and neonatal liver failure.
    Heissat S, Collardeau-Frachon S, Baruteau J, Dubruc E, Bouvier R, Fabre M, Cordier MP, Broué P, Guigonis V, Debray D.
    J Pediatr; 2015 Jan 20; 166(1):66-73. PubMed ID: 25444000
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  • 37. Depletion of mitochondrial DNA by down-regulation of deoxyguanosine kinase expression in non-proliferating HeLa cells.
    Franco M, Johansson M, Karlsson A.
    Exp Cell Res; 2007 Jul 15; 313(12):2687-94. PubMed ID: 17490647
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  • 38. Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure.
    Al-Hussaini A, Faqeih E, El-Hattab AW, Alfadhel M, Asery A, Alsaleem B, Bakhsh E, Ali A, Alasmari A, Lone K, Nahari A, Eyaid W, Al Balwi M, Craig K, Butterworth A, He L, Taylor RW.
    J Pediatr; 2014 Mar 15; 164(3):553-9.e1-2. PubMed ID: 24321534
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  • 39. A novel c.592-4_c.592-3delTT mutation in DGUOK gene causes exon skipping.
    Ji JQ, Dimmock D, Tang LY, Descartes M, Gomez R, Rutledge SL, Schmitt ES, Wong LJ.
    Mitochondrion; 2010 Mar 15; 10(2):188-91. PubMed ID: 19900589
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  • 40. Labial salivary gland involvement in neonatal hemochromatosis: a report of 2 cases and review of literature.
    Chan KC, Edelman M, Fantasia JE.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Jul 15; 106(1):e27-30. PubMed ID: 18585608
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