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For: Chinnery PF. Mutations in SUCLA2: a tandem ride back to the Krebs cycle. Brain 2007;130:606-9. [DOI: 10.1093/brain/awm023] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Chinopoulos C. The "B space" of mitochondrial phosphorylation. J Neurosci Res 2011;89:1897-904. [PMID: 21541983 DOI: 10.1002/jnr.22659] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 2.3] [Reference Citation Analysis]
2 Couser NL, Marchuk DS, Smith LD, Arreola A, Kaiser-Rogers KA, Muenzer J, Pandya A, Gucsavas-Calikoglu M, Powell CM. Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome. Am J Med Genet A 2017;173:2720-4. [PMID: 28749033 DOI: 10.1002/ajmg.a.38351] [Cited by in Crossref: 2] [Article Influence: 0.4] [Reference Citation Analysis]
3 Bornstein B, Area E, Flanigan KM, Ganesh J, Jayakar P, Swoboda KJ, Coku J, Naini A, Shanske S, Tanji K, Hirano M, DiMauro S. Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscul Disord 2008;18:453-9. [PMID: 18504129 DOI: 10.1016/j.nmd.2008.04.006] [Cited by in Crossref: 62] [Cited by in F6Publishing: 50] [Article Influence: 4.4] [Reference Citation Analysis]
4 Shan SW, Tse DY, Zuo B, To CH, Liu Q, McFadden SA, Chun RK, Bian J, Li KK, Lam TC. Integrated SWATH-based and targeted-based proteomics provide insights into the retinal emmetropization process in guinea pig. J Proteomics 2018;181:1-15. [PMID: 29572162 DOI: 10.1016/j.jprot.2018.03.023] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 3.5] [Reference Citation Analysis]
5 Valayannopoulos V, Haudry C, Serre V, Barth M, Boddaert N, Arnoux JB, Cormier-Daire V, Rio M, Rabier D, Vassault A, Munnich A, Bonnefont JP, de Lonlay P, Rötig A, Lebre AS. New SUCLG1 patients expanding the phenotypic spectrum of this rare cause of mild methylmalonic aciduria. Mitochondrion 2010;10:335-41. [PMID: 20197121 DOI: 10.1016/j.mito.2010.02.006] [Cited by in Crossref: 34] [Cited by in F6Publishing: 27] [Article Influence: 2.8] [Reference Citation Analysis]
6 Güngör O, Özkaya AK, Güngör G, Karaer K, Dilber C, Aydin K. Novel mutation in SUCLA2 identified on sequencing analysis. Pediatr Int 2016;58:659-61. [PMID: 26952923 DOI: 10.1111/ped.12921] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]