Mutations in Assembly Factors Required for the Biogenesis of Mitochondrial Respiratory Chain
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-70147-5_2
Reference234 articles.
1. Agip AA, Blaza JN, Fedor JG, Hirst J (2019) Mammalian respiratory complex I through the lens of Cryo-EM. Annu Rev Biophys 48:165–184
2. Alcazar-Fabra M, Trevisson E, Brea-Calvo G (2018) Clinical syndromes associated with coenzyme Q10 deficiency. Essays Biochem 62:377–398
3. Alfadhel M, Lillquist YP, Waters PJ, Sinclair G, Struys E, Mcfadden D, Hendson G, Hyams L, Shoffner J, Vallance HD (2011) Infantile cardioencephalopathy due to a COX15 gene defect: report and review. Am J Med Genet A 155A:840–844
4. Alston CL, Davison JE, Meloni F, van der Westhuizen FH, He L, Hornig-Do HT, Peet AC, Gissen P, Goffrini P, Ferrero I, Wassmer E, Mcfarland R, Taylor RW (2012) Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency. J Med Genet 49:569–577
5. Alston CL, Ceccatelli Berti C, Blakely EL, Olahova M, He L, Mcmahon CJ, Olpin SE, Hargreaves IP, Nolli C, Mcfarland R, Goffrini P, O’sullivan MJ, Taylor RW (2015) A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Hum Genet 134:869–879
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