OPA3 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "OPA3" in Arabic language version.

Last modified: 02:45:00, 1 December 2025 (UTC)

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Nystuen A، Costeff H، Elpeleg ON، Apter N، Bonne-Tamir B، Mohrenweiser H، Haider N، Stone EM، Sheffield VC (يوليو 1997). "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". Hum Mol Genet. ج. 6 ع. 4: 563–9. DOI:10.1093/hmg/6.4.563. PMID:9097959.
Anikster Y، Kleta R، Shaag A، Gahl WA، Elpeleg O (نوفمبر 2001). "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". Am J Hum Genet. ج. 69 ع. 6: 1218–24. DOI:10.1086/324651. PMC:1235533. PMID:11668429.
Wells T، Davies JR، Guschina IA، Ball DJ، Davies JS، Davies VJ، وآخرون (نوفمبر 2012). "Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome". Human Molecular Genetics. ج. 21 ع. 22: 4836–4844. DOI:10.1093/hmg/dds315. PMID:22869679.

Nystuen A، Costeff H، Elpeleg ON، Apter N، Bonne-Tamir B، Mohrenweiser H، Haider N، Stone EM، Sheffield VC (يوليو 1997). "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". Hum Mol Genet. ج. 6 ع. 4: 563–9. DOI:10.1093/hmg/6.4.563. PMID:9097959.
Anikster Y، Kleta R، Shaag A، Gahl WA، Elpeleg O (نوفمبر 2001). "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". Am J Hum Genet. ج. 69 ع. 6: 1218–24. DOI:10.1086/324651. PMC:1235533. PMID:11668429.
Wells T، Davies JR، Guschina IA، Ball DJ، Davies JS، Davies VJ، وآخرون (نوفمبر 2012). "Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome". Human Molecular Genetics. ج. 21 ع. 22: 4836–4844. DOI:10.1093/hmg/dds315. PMID:22869679.

"Costeff syndrome". Genetics Home Reference. مؤرشف من الأصل في 2020-09-20. اطلع عليه بتاريخ 2017-05-28.

"Entrez Gene: OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)". مؤرشف من الأصل في 2010-04-10.
"Costeff syndrome". Genetics Home Reference. مؤرشف من الأصل في 2020-09-20. اطلع عليه بتاريخ 2017-05-28.