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Glad to be part of international efforts that led to the discovery of 3 new genetic syndromes: FBXO11 (https://t.co/CuK9pe63zs ), BCL11B (https://t.co/C1TC9BHbDI ) and CACNA1G (https://t.co/QBYWLAt7Iz)
Glad to be part of international efforts that led to the discovery of 3 new genetic syndromes: FBXO11 (https://t.co/CuK9pe63zs ), BCL11B (https://t.co/C1TC9BHbDI ) and CACNA1G (https://t.co/QBYWLAt7Iz)
RT @insb_cnrs: Des mutations "gain de fonction" d’un canal calcique dans l'atrophie cérébelleuse de l’enfant ➡️ https://t.co/3HOjfPYHpH 📕 h…
RT @CNRS: #EnDirectDesLabos🔎 | Des #mutations "gain de fonction" d’un canal calcique dans l'atrophie cérébelleuse de l’enfant 🧠🧒 ➡️ https:…