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Correction to: Clinical and genetic aspects of defects in the mitochondrial iron-sulfur cluster synthesis pathway.
Vanlander AV, Van Coster R. Vanlander AV, et al. Among authors: van coster r. J Biol Inorg Chem. 2018 Jun;23(4):507. doi: 10.1007/s00775-018-1564-6. J Biol Inorg Chem. 2018. PMID: 29855714 Free PMC article.
The article "Clinical and genetic aspects of defects in the mitochondrial iron-sulfur cluster synthesis pathway", written by A. V. Vanlander, R. Van Coster was originally published....
The article "Clinical and genetic aspects of defects in the mitochondrial iron-sulfur cluster synthesis pathway", written by A. V. Vanlander …
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency.
Ahting U, Mayr JA, Vanlander AV, Hardy SA, Santra S, Makowski C, Alston CL, Zimmermann FA, Abela L, Plecko B, Rohrbach M, Spranger S, Seneca S, Rolinski B, Hagendorff A, Hempel M, Sperl W, Meitinger T, Smet J, Taylor RW, Van Coster R, Freisinger P, Prokisch H, Haack TB. Ahting U, et al. Among authors: van coster r. Front Genet. 2015 Apr 13;6:123. doi: 10.3389/fgene.2015.00123. eCollection 2015. Front Genet. 2015. PMID: 25918518 Free PMC article.
Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency.
Vantroys E, Smet J, Vanlander AV, Vergult S, De Bruyne R, Roels F, Stepman H, Roeyers H, Menten B, Van Coster R. Vantroys E, et al. Among authors: van coster r. Orphanet J Rare Dis. 2018 May 21;13(1):80. doi: 10.1186/s13023-018-0822-6. Orphanet J Rare Dis. 2018. PMID: 29783990 Free PMC article.
Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy.
Ajit Bolar N, Vanlander AV, Wilbrecht C, Van der Aa N, Smet J, De Paepe B, Vandeweyer G, Kooy F, Eyskens F, De Latter E, Delanghe G, Govaert P, Leroy JG, Loeys B, Lill R, Van Laer L, Van Coster R. Ajit Bolar N, et al. Among authors: van der aa n, van coster r, van laer l. Hum Mol Genet. 2013 Jul 1;22(13):2590-602. doi: 10.1093/hmg/ddt107. Epub 2013 Mar 5. Hum Mol Genet. 2013. PMID: 23462291
204 results