Found 8 results
Filters: Author is Le Scouarnec, Solena  [Clear All Filters]
2018
[Anonymous].  2018.  Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm. The American Journal of Human Genetics. 102:133–141.
2015
[Anonymous].  2015.  Fine-scale human genetic structure in Western France. European Journal of Human Genetics. 23:831–836.
[Anonymous].  2015.  Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human Molecular Genetics. 24:2757–2763.
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