Leigh syndrome, French Canadian type (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Leigh syndrome, French Canadian type" in English language version.

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Cooper, Marcus P.; Qu, Lishu; Rohas, Lindsay M.; Lin, Jiandie; Yang, Wenli; Erdjument-Bromage, Hediye; Tempst, Paul; Spiegelman, Bruce M. (2006-11-01). "Defects in energy homeostasis in Leigh syndrome French Canadian variant through PGC-1α/LRP130 complex". Genes & Development. 20 (21): 2996–3009. doi:10.1101/gad.1483906. ISSN 0890-9369. PMC 1620022. PMID 17050673.
Lee, N.; Daly, M. J.; Delmonte, T.; Lander, E. S.; Xu, F.; Hudson, T. J.; Mitchell, G. A.; Morin, C. C.; Robinson, B. H.; Rioux, J. D. (February 2001). "A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16". American Journal of Human Genetics. 68 (2): 397–409. doi:10.1086/318197. ISSN 0002-9297. PMC 1235273. PMID 11156535.

Cooper, Marcus P.; Qu, Lishu; Rohas, Lindsay M.; Lin, Jiandie; Yang, Wenli; Erdjument-Bromage, Hediye; Tempst, Paul; Spiegelman, Bruce M. (2006-11-01). "Defects in energy homeostasis in Leigh syndrome French Canadian variant through PGC-1α/LRP130 complex". Genes & Development. 20 (21): 2996–3009. doi:10.1101/gad.1483906. ISSN 0890-9369. PMC 1620022. PMID 17050673.
Lee, N.; Daly, M. J.; Delmonte, T.; Lander, E. S.; Xu, F.; Hudson, T. J.; Mitchell, G. A.; Morin, C. C.; Robinson, B. H.; Rioux, J. D. (February 2001). "A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16". American Journal of Human Genetics. 68 (2): 397–409. doi:10.1086/318197. ISSN 0002-9297. PMC 1235273. PMID 11156535.
Merante, F.; Petrova-Benedict, R.; MacKay, N.; Mitchell, G.; Lambert, M.; Morin, C.; De Braekeleer, M.; Laframboise, R.; Gagné, R.; Robinson, B. H. (August 1993). "A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec". American Journal of Human Genetics. 53 (2): 481–487. ISSN 0002-9297. PMC 1682348. PMID 8392290.

Cooper, Marcus P.; Qu, Lishu; Rohas, Lindsay M.; Lin, Jiandie; Yang, Wenli; Erdjument-Bromage, Hediye; Tempst, Paul; Spiegelman, Bruce M. (2006-11-01). "Defects in energy homeostasis in Leigh syndrome French Canadian variant through PGC-1α/LRP130 complex". Genes & Development. 20 (21): 2996–3009. doi:10.1101/gad.1483906. ISSN 0890-9369. PMC 1620022. PMID 17050673.
Lee, N.; Daly, M. J.; Delmonte, T.; Lander, E. S.; Xu, F.; Hudson, T. J.; Mitchell, G. A.; Morin, C. C.; Robinson, B. H.; Rioux, J. D. (February 2001). "A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16". American Journal of Human Genetics. 68 (2): 397–409. doi:10.1086/318197. ISSN 0002-9297. PMC 1235273. PMID 11156535.
Merante, F.; Petrova-Benedict, R.; MacKay, N.; Mitchell, G.; Lambert, M.; Morin, C.; De Braekeleer, M.; Laframboise, R.; Gagné, R.; Robinson, B. H. (August 1993). "A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec". American Journal of Human Genetics. 53 (2): 481–487. ISSN 0002-9297. PMC 1682348. PMID 8392290.

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Congenital lactic acidosis Saguenay Lac Saint Jean type Leigh syndrome French Canadian type". www.orpha.net. Retrieved 2022-05-19.{{cite web}}: CS1 maint: numeric names: authors list (link)

Cooper, Marcus P.; Qu, Lishu; Rohas, Lindsay M.; Lin, Jiandie; Yang, Wenli; Erdjument-Bromage, Hediye; Tempst, Paul; Spiegelman, Bruce M. (2006-11-01). "Defects in energy homeostasis in Leigh syndrome French Canadian variant through PGC-1α/LRP130 complex". Genes & Development. 20 (21): 2996–3009. doi:10.1101/gad.1483906. ISSN 0890-9369. PMC 1620022. PMID 17050673.
Lee, N.; Daly, M. J.; Delmonte, T.; Lander, E. S.; Xu, F.; Hudson, T. J.; Mitchell, G. A.; Morin, C. C.; Robinson, B. H.; Rioux, J. D. (February 2001). "A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16". American Journal of Human Genetics. 68 (2): 397–409. doi:10.1086/318197. ISSN 0002-9297. PMC 1235273. PMID 11156535.
Merante, F.; Petrova-Benedict, R.; MacKay, N.; Mitchell, G.; Lambert, M.; Morin, C.; De Braekeleer, M.; Laframboise, R.; Gagné, R.; Robinson, B. H. (August 1993). "A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec". American Journal of Human Genetics. 53 (2): 481–487. ISSN 0002-9297. PMC 1682348. PMID 8392290.