Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews (Q24291826)

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Language	Label	Description	Also known as
English	Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews	scientific article

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scholarly article

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Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews (English)

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Outer mitochondrial membrane lipid metabolism regulator OPA3

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GOA release 2020-03-11

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based on heuristic

inferred from title

3-methylglutaconic aciduria

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based on heuristic

inferred from title

author name string

Y Anikster

1

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R Kleta

2

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A Shaag

3

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W A Gahl

4

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O Elpeleg

5

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language of work or name

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publication date

December 2001

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American Journal of Human Genetics

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69

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6

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1218-24

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

1 reference

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19 March 2017

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

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19 March 2017

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

1 reference

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19 March 2017

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

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19 March 2017

Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria

1 reference

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19 March 2017

A conserved tripeptide sorts proteins to peroxisomes

1 reference

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7 April 2017

Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups

1 reference

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27 September 2017

Molecular basis of mendelian disorders among Jews

1 reference

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27 September 2017

Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene

1 reference

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27 September 2017

Multiple syndromes of 3-methylglutaconic aciduria

1 reference

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27 September 2017

Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations

1 reference

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27 September 2017

3-Hydroxy-3-methylglutaryl-CoA lyase is present in mouse and human liver peroxisomes

1 reference

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27 September 2017

3-Methylglutaconic aciduria in the Iraqi-Jewish 'optic atrophy plus' (Costeff) syndrome

1 reference

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27 September 2017

A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia

1 reference

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27 September 2017

3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects

1 reference

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27 September 2017

Ineffectiveness of oral coenzyme Q10 supplementation in 3-methylglutaconic aciduria, type 3.

1 reference

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30 May 2018

3-Methylglutaconic aciduria in "optic atrophy plus".

1 reference

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30 May 2018

3-Methylglutaconic Acidemia in Smith-Lemli-Opitz Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235533

30 May 2018

Transfer of carbon atoms from mevalonate to n-fatty acids

1 reference

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30 May 2018

Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria

1 reference

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29 November 2018

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

1 reference

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29 November 2018

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial complex deficiencies in a male with cardiomyopathy and 3-methylglutaconic aciduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/11668429

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

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ResearchGate publication ID

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