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Year | Number of Results |
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2010 | 1 |
2013 | 1 |
2014 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (cited) for id: 614585
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A novel complex neurological phenotype due to a homozygous mutation in FDX2.
Brain. 2018 Aug 1;141(8):2289-2298. doi: 10.1093/brain/awy172.
Brain. 2018.
PMID: 30010796
Free PMC article.
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.
Spiegel R, Saada A, Halvardson J, Soiferman D, Shaag A, Edvardson S, Horovitz Y, Khayat M, Shalev SA, Feuk L, Elpeleg O.
Spiegel R, et al.
Eur J Hum Genet. 2014 Jul;22(7):902-6. doi: 10.1038/ejhg.2013.269. Epub 2013 Nov 27.
Eur J Hum Genet. 2014.
PMID: 24281368
Free PMC article.
Clinical Trial.
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Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis.
Sheftel AD, Stehling O, Pierik AJ, Elsässer HP, Mühlenhoff U, Webert H, Hobler A, Hannemann F, Bernhardt R, Lill R.
Sheftel AD, et al.
Proc Natl Acad Sci U S A. 2010 Jun 29;107(26):11775-80. doi: 10.1073/pnas.1004250107. Epub 2010 Jun 14.
Proc Natl Acad Sci U S A. 2010.
PMID: 20547883
Free PMC article.
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