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SC
Sandrine Couvet
Ingénieure d'Etudes
33%
Libre accès
3
Documents
Affiliations actuelles
- 1081006
Identifiants chercheurs
- sandrine-couvet
- 0000-0003-3676-1891
- ResearcherId : HKE-8103-2023
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TTC12 loss-of-function mutations cause primary Ciliary Dyskinesia and unveil distinct dynein assembly mechanisms in motile cilia versus flagellaAmerican Journal of Human Genetics, 2020, 106 (2), pp.153-169. ⟨10.1016/j.ajhg.2019.12.010⟩
Article dans une revue
hal-02456263v1
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TTC12 loss-of-function mutations cause primary ciliary dyskinesia and unveil distinct dynein assembly mechanisms in motile cilia versus flagellaAssises de Génétique, Feb 2022, Rennes (FR), France
Communication dans un congrès
inserm-03922541v1
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TTC12 loss-of-function mutations cause primary ciliary dyskinesia and unveil distinct dynein assembly mechanisms in motile cilia versus flagellaESHG 2022, Jun 2022, Vienne, Austria
Poster de conférence
inserm-03845363v1
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