A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome-Reference-Cited by-同舟云学术

A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome

Published:2015-11 Issue: Volume:25 Page:113-119
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Duff Rachael M.,Shearwood Anne-Marie J.,Ermer Judith,Rossetti Giulia,Gooding Rebecca,Richman Tara R.,Balasubramaniam Shanti,Thorburn David R.,Rackham Oliver,Lamont Phillipa J.,Filipovska Aleksandra

Funder

National Health and Medical Research Council

Australian Mitochondrial Disease Foundation (AMDF)

NHMRC

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference32 articles.

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3. Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA;Bindoff,1993

4. Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease;Blakely;Hum. Mutat.,2013

5. Mitochondria: impaired mitochondrial translation in human disease;Boczonadi;Int. J. Biochem. Cell Biol.,2014

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