Cited by

• Gastrointestinal and hepatic manifestations of mitochondrial disorders.

  Rahman S. Rahman S. J Inherit Metab Dis. 2013 Jul;36(4):659-73. doi: 10.1007/s10545-013-9614-2. Epub 2013 May 15. J Inherit Metab Dis. 2013. PMID: 23674168 Review.
• Insertion of an LrDNA gene fragment and of filler DNA at a mitochondrial exon-intron junction in Podospora.

  Sainsard-Chanet A, Begel O. Sainsard-Chanet A, et al. Nucleic Acids Res. 1990 Feb 25;18(4):779-83. doi: 10.1093/nar/18.4.779. Nucleic Acids Res. 1990. PMID: 2156230 Free PMC article.
• Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.

  Cormier V, Rotig A, Tardieu M, Colonna M, Saudubray JM, Munnich A. Cormier V, et al. Am J Hum Genet. 1991 Apr;48(4):643-8. Am J Hum Genet. 1991. PMID: 2014791 Free PMC article.
• Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndrome.

  Niaudet P, Heidet L, Munnich A, Schmitz J, Bouissou F, Gubler MC, Rötig A. Niaudet P, et al. Pediatr Nephrol. 1994 Apr;8(2):164-8. doi: 10.1007/BF00865468. Pediatr Nephrol. 1994. PMID: 8018492
• Engineering mtDNA deletions by reconstituting end joining in human mitochondria.

  Fu Y, Land M, Kavlashvili T, Cui R, Kim M, DeBitetto E, Lieber T, Ryu KW, Choi E, Masilionis I, Saha R, Takizawa M, Baker D, Tigano M, Lareau CA, Reznik E, Sharma R, Chaligne R, Thompson CB, Pe'er D, Sfeir A. Fu Y, et al. Cell. 2025 May 15;188(10):2778-2793.e21. doi: 10.1016/j.cell.2025.02.009. Epub 2025 Mar 10. Cell. 2025. PMID: 40068680