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Page 1
Diseases of the human mitochondrial oxidative phosphorylation system.
Adv Exp Med Biol. 2009;652:47-67. doi: 10.1007/978-90-481-2813-6_5.
Adv Exp Med Biol. 2009.
PMID: 20225019
Review.
New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy.
Martínez-Romero Í, Herrero-Martín MD, Llobet L, Emperador S, Martín-Navarro A, Narberhaus B, Ascaso FJ, López-Gallardo E, Montoya J, Ruiz-Pesini E.
Martínez-Romero Í, et al. Among authors: herrero martin md.
Clin Exp Ophthalmol. 2014 Dec;42(9):856-64. doi: 10.1111/ceo.12355. Epub 2014 May 30.
Clin Exp Ophthalmol. 2014.
PMID: 24800637
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A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation.
Herrero-Martín MD, Ayuso T, Tuñón MT, Martín MA, Ruiz-Pesini E, Montoya J.
Herrero-Martín MD, et al.
J Neurol Neurosurg Psychiatry. 2010 Apr;81(4):471-2. doi: 10.1136/jnnp.2009.173831.
J Neurol Neurosurg Psychiatry. 2010.
PMID: 20360171
No abstract available.
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A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1).
Herrero-Martín MD, Pineda M, Briones P, López-Gallardo E, Carreras M, Benac M, Angel Idoate M, Vilaseca MA, Artuch R, López-Pérez MJ, Ruiz-Pesini E, Montoya J.
Herrero-Martín MD, et al.
Hum Mutat. 2008 Aug;29(8):E112-22. doi: 10.1002/humu.20800.
Hum Mutat. 2008.
PMID: 18484665
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NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein.
López-Gallardo E, Solano A, Herrero-Martín MD, Martínez-Romero I, Castaño-Pérez MD, Andreu AL, Herrera A, López-Pérez MJ, Ruiz-Pesini E, Montoya J.
López-Gallardo E, et al. Among authors: herrero martin md.
J Med Genet. 2009 Jan;46(1):64-7. doi: 10.1136/jmg.2008.060616.
J Med Genet. 2009.
PMID: 19124644
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