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Year | Number of Results |
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2015 | 1 |
2017 | 1 |
2023 | 1 |
2024 | 0 |
PubMed for id: 1643082
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A neuron-specific Isca1 knockout rat developments multiple mitochondrial dysfunction syndromes.
Animal Model Exp Med. 2023 Apr;6(2):155-167. doi: 10.1002/ame2.12318.
Animal Model Exp Med. 2023.
PMID: 37140997
Free PMC article.
Understanding the Molecular Basis of Multiple Mitochondrial Dysfunctions Syndrome 1 (MMDS1)-Impact of a Disease-Causing Gly208Cys Substitution on Structure and Activity of NFU1 in the Fe/S Cluster Biosynthetic Pathway.
Wachnowsky C, Wesley NA, Fidai I, Cowan JA.
Wachnowsky C, et al.
J Mol Biol. 2017 Mar 24;429(6):790-807. doi: 10.1016/j.jmb.2017.01.021. Epub 2017 Feb 1.
J Mol Biol. 2017.
PMID: 28161430
Free PMC article.
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.
Debray FG, Stümpfig C, Vanlander AV, Dideberg V, Josse C, Caberg JH, Boemer F, Bours V, Stevens R, Seneca S, Smet J, Lill R, van Coster R.
Debray FG, et al.
J Inherit Metab Dis. 2015 Nov;38(6):1147-53. doi: 10.1007/s10545-015-9857-1. Epub 2015 May 14.
J Inherit Metab Dis. 2015.
PMID: 25971455
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