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PubMed (cited) for id: 607571
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Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease.
Genet Med. 2019 Sep;21(9):2163-2164. doi: 10.1038/s41436-019-0506-1.
Genet Med. 2019.
PMID: 31028354
Free PMC article.
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly.
Meyertholen K, Ravnan JB, Matalon R.
Meyertholen K, et al.
Mol Syndromol. 2012 Jun;3(1):25-9. doi: 10.1159/000339177. Epub 2012 Jun 13.
Mol Syndromol. 2012.
PMID: 25759628
Free PMC article.
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Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.
Maguire S, Estabel J, Ingham N, Pearson S, Ryder E, Carragher DM, Walker N; Sanger MGP Slc25a21 Project Team; Bussell J, Chan WI, Keane TM, Adams DJ, Scudamore CL, Lelliott CJ, Ramírez-Solis R, Karp NA, Steel KP, White JK, Gerdin AK.
Maguire S, et al.
PLoS One. 2014 Mar 18;9(3):e91807. doi: 10.1371/journal.pone.0091807. eCollection 2014.
PLoS One. 2014.
PMID: 24642684
Free PMC article.
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Identification of Cis-regulatory elements in the mouse Pax9/Nkx2-9 genomic region: implication for evolutionary conserved synteny.
Santagati F, Abe K, Schmidt V, Schmitt-John T, Suzuki M, Yamamura K, Imai K.
Santagati F, et al.
Genetics. 2003 Sep;165(1):235-42. doi: 10.1093/genetics/165.1.235.
Genetics. 2003.
PMID: 14504231
Free PMC article.
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Identification of the human mitochondrial oxodicarboxylate carrier. Bacterial expression, reconstitution, functional characterization, tissue distribution, and chromosomal location.
Fiermonte G, Dolce V, Palmieri L, Ventura M, Runswick MJ, Palmieri F, Walker JE.
Fiermonte G, et al.
J Biol Chem. 2001 Mar 16;276(11):8225-30. doi: 10.1074/jbc.M009607200. Epub 2000 Nov 16.
J Biol Chem. 2001.
PMID: 11083877
Free article.
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