Département Génétique Médicale, Maladies rares et médecine personnalisée

Research facility


Location: Montpellier, France (FR) FR

ISNI: -

De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder (2019) Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, et al. Journal article