Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes
Mounia Bensaid, Yann Loe-Mie, Aude-Marie Lepagnol-Bestel, Wenqi Han, Gabriel Santpere, Thomas Klarić, Christine Plançon, Rim Roudies, Imane Benhima, Nisrine Tarik, Patrick Nitschké, Jean-Marc Plaza, Hassan Kisra, Jean‐François Deleuze, Nenad Šestan, , Michel Simonneau
The paper identifies a multi-hit genomic architecture for ASD in consanguineous families, involving FEZF2 deletions and mutations in high-risk genes.
bioRxiv · Sep 11, 2019 · PreprintNeuroscience