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

Publié le 2 octobre 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
Institut
IG
Département / Service
IG/CNG
Laboratoire
LMPD
Date de création 
Facteur Impact 
url DOI10.1038/ejhg.2013.135

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