Florence Riant
4PUBLICATIONS
8CO-AUTHORS

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Publications (4)
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|May 16, 2024
Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations.Annabelle Chaussenot, Xavier Ayrignac, Nicolas Chatron
|Jan 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations.Françoise Bergametti, Geraldine Viot, Christophe Verny
|Jan 12, 2020
Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome.Chaker Aloui, Stéphanie Guey, Eva Pipiras
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