Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations

Disorders caused by defects in the mitochondrial translation system are clinically and genetically heterogeneous. The elongation phase of mitochondrial protein synthesis requires, among many other components, three nuclear-encoded elongation factors: EFTu (TUFM; 602389), EFTs (TSFM; 604723), and EFG...

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Detalles Bibliográficos
Autores principales: Ravn, Kirstine, Schönewolf-Greulich, Bitten, Hansen, Rikke M., Bohr, Anna-Helene, Duno, Morten, Wibrand, Flemming, Ostergaard, Elsebet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750589/
https://www.ncbi.nlm.nih.gov/pubmed/26937387
http://dx.doi.org/10.1016/j.ymgmr.2015.01.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750589/
https://www.ncbi.nlm.nih.gov/pubmed/26937387
http://dx.doi.org/10.1016/j.ymgmr.2015.01.004

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