Aurore Despres

Aurore Despres

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Aurore Despres

Aurore Despres

Publications by authors named "Aurore Despres"

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Intragenic deletion of the WDR45 gene in a male with encephalopathy, severe psychomotor disability, and epilepsy.

Am J Med Genet A 2017 May 3;173(5):1444-1446. Epub 2017 Apr 3.

Laboratoire de génétique moléculaire et d'histocompatibilité, CHRU Morvan, Brest, France.

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http://dx.doi.org/10.1002/ajmg.a.38180DOI Listing
May 2017

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

Nat Genet 2013 Sep 21;45(9):1044-9. Epub 2013 Jul 21.

Department of Clinical and Experimental Cardiology, Heart Failure Research Center, Academic Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1038/ng.2712DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869788PMC
September 2013