You are here : Home > AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)

Publications CNRGH

AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)

Published on 2 October 2023
AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
Description
 
Date de publication 
Auteurs
Cacciagli P, Desvignes JP, Girard N, Delepine M, Zelenika D, Lathrop M, Levy N, Ledbetter DH, Dobyns WB and Villard L
Revue
Année2,014
Département / Service
IG/CNG
Laboratoire
LMPD
Impact Factor 
Institut IG
url DOI10.1038/ejhg.2013.135

Retour à la liste