| Zeit | ID | Programmpunkt | ||
|---|---|---|---|---|
|
17.03.2022
10:15–10:30 |
W2-002 |
FBXO11 haploinsufficiency also stems from de novo missense variants and impairs neuronal differentiation and migration in an iPSC-based neuronal model | ||
|
17.03.2022
16:45–17:00 |
W6-004 |
Pathogenic variants of CSNK2B cause a distinguished intellectual disability-craniodigital syndrome by interrupting canonical Wnt signaling pathway |