PARS2-associated mitochondrial disease: A case report of a patient with prolonged survival and literature review

Author:

A. Almuqbil Mohammed,Vernon Hilary J.,Ferguson Marcia,Kline Antonie D.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference14 articles.

1. Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases;Suzuki;Annu. Rev. Genet.,2011

2. Aminoacyl-tRNA synthetase complexes in evolution;Havrylenko;Int. J. Mol. Sci.,2015

3. Aminoacyl-tRNA synthetases in biology and disease: new evidence for structural and functional diversity in an ancient family of enzymes;Francklyn;RNA,1997

4. Significance of mitochondria DNA mutations in diseases;Zhu;Adv. Exp. Med. Biol.,2017

5. Mechanisms of mitochondrial diseases;Ylikallio;Ann. Med.,2012

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