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Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation

  • Published:2017-04 Issue:4 Volume:1863 Page:961-967
  • ISSN:0925-4439
  • Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  • language:en
  • Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Di Nottia Michela,Montanari Arianna,Verrigni Daniela,Oliva Romina,Torraco Alessandra,Fernandez-Vizarra Erika,Diodato Daria,Rizza Teresa,Bianchi Marzia,Catteruccia Michela,Zeviani Massimo,Dionisi-Vici Carlo,Francisci Silvia,Bertini Enrico,Carrozzo Rosalba

Funder

Telethon Grant

Italian Ministry of Health

Pasteur Institute - Cenci Bolognetti Foundation

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference27 articles.

1. Mitochondrial DNA and disease;Greaves;J. Pathol.,2012

2. Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies;Smits;J. Biomed. Biotechnol.,2010

3. 175th ENMC International Workshop: mitochondrial protein synthesis in health and disease;Chrzanowska-Lightowlers;Neuromuscul. Disord.,2011

4. Human diseases with impaired mitochondrial protein synthesis;Rötig;Biochim. Biophys. Acta,1807

5. Mitochondrial disorders as windows into an ancient organelle;Vafai;Nature,2012

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