(Q49291677)

19 February 2018

title

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. (English)

1 reference

19 February 2018

0 references

1 reference

mitochondrial disease

1 reference

Taylor RW

1

1 reference

19 February 2018

Singh-Kler R

2

1 reference

19 February 2018

Hayes CM

3

1 reference

19 February 2018

Smith PE

4

1 reference

19 February 2018

Turnbull DM

5

1 reference

19 February 2018

publication date

1 July 2001

1 reference

19 February 2018

published in

Annals of Neurology

1 reference

19 February 2018

volume

50

1 reference

19 February 2018

issue

1

1 reference

19 February 2018

page(s)

104-107

1 reference

19 February 2018

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

cites work

1 reference

Leber hereditary optic neuropathy: how do mitochondrial DNA mutations cause degeneration of the optic nerve?

21 January 2018

1 reference

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

21 January 2018

1 reference

Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene.

21 January 2018

1 reference

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

21 January 2018

1 reference

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

21 January 2018

1 reference

Conservation of sequences of subunits of mitochondrial complex I and their relationships with other proteins

21 January 2018

1 reference

The protein information resource (PIR)

21 January 2018

1 reference

Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

21 January 2018

1 reference

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy

21 January 2018

1 reference

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.1084

1 reference

19 February 2018

PubMed ID

11456298

1 reference

19 February 2018