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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2004 | 1 |
2007 | 1 |
2009 | 1 |
2011 | 1 |
2024 | 0 |
PubMed (cited) for id: 301020
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Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency.
Mol Genet Metab. 2011 Aug;103(4):358-61. doi: 10.1016/j.ymgme.2011.04.010. Epub 2011 May 5.
Mol Genet Metab. 2011.
PMID: 21596602
A novel NDUFA1 mutation leads to a progressive mitochondrial complex I-specific neurodegenerative disease.
Potluri P, Davila A, Ruiz-Pesini E, Mishmar D, O'Hearn S, Hancock S, Simon M, Scheffler IE, Wallace DC, Procaccio V.
Potluri P, et al.
Mol Genet Metab. 2009 Apr;96(4):189-95. doi: 10.1016/j.ymgme.2008.12.004. Epub 2009 Jan 29.
Mol Genet Metab. 2009.
PMID: 19185523
Free PMC article.
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X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.
Fernandez-Moreira D, Ugalde C, Smeets R, Rodenburg RJ, Lopez-Laso E, Ruiz-Falco ML, Briones P, Martin MA, Smeitink JA, Arenas J.
Fernandez-Moreira D, et al.
Ann Neurol. 2007 Jan;61(1):73-83. doi: 10.1002/ana.21036.
Ann Neurol. 2007.
PMID: 17262856
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SOD2 gene transfer protects against optic neuropathy induced by deficiency of complex I.
Qi X, Lewin AS, Sun L, Hauswirth WW, Guy J.
Qi X, et al.
Ann Neurol. 2004 Aug;56(2):182-91. doi: 10.1002/ana.20175.
Ann Neurol. 2004.
PMID: 15293270
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