(Q82023250)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's ataxia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference

1 reference

Mohammad Mehdi Heidari

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Shahriar Nafissi

4

1 reference

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14 January 2020

author name string

Massoud Houshmand

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Saman Hosseinkhani

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Barbara Scheiber-Mojdehkar

5

1 reference

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14 January 2020

Mehri Khatami

6

1 reference

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14 January 2020

publication date

19 September 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

Cellular and Molecular Neurobiology

14 January 2020

published in

1 reference

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14 January 2020

volume

29

1 reference

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14 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

page(s)

225-233

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18807169%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10571-008-9315-9

14 January 2020

exact match

0 references

cites work

Sequence and organization of the human mitochondrial genome

1 reference

12 December 2020

Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer

1 reference

12 December 2020

Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia

1 reference

12 December 2020

Mitochondrial control of iron homeostasis. A genome wide analysis of gene expression in a yeast frataxin-deficient strain

1 reference

12 December 2020

Comprehensive scanning of the entire mitochondrial genome for mutations.

1 reference

12 December 2020

Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations

1 reference

12 December 2020

Deletion of the yeast homologue of the human gene associated with Friedreich's ataxia elicits iron accumulation in mitochondria

1 reference

12 December 2020

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

12 December 2020

Brain Cytochrome Oxidase in Alzheimer's Disease

1 reference

12 December 2020

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis

1 reference

12 December 2020

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

12 December 2020

Mitochondrial functional interactions between frataxin and Isu1p, the iron-sulfur cluster scaffold protein, in Saccharomyces cerevisiae

1 reference

12 December 2020

Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin

1 reference

12 December 2020

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

Nitric oxide, mitochondria and neurological disease

1 reference

12 December 2020

Human mitochondrial complex I dysfunction

1 reference

12 December 2020

Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

1 reference

12 December 2020

Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.

1 reference

12 December 2020

Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia

1 reference

12 December 2020

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

12 December 2020