AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome) - Aix-Marseille Université Access content directly
Journal Articles European Journal of Human Genetics Year : 2013

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

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hal-01668667 , version 1 (20-12-2017)

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Pierre Cacciagli, Jean-Pierre Desvignes, Nadine Girard, Marc Délépine, Diana Zelenika, et al.. AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). European Journal of Human Genetics, 2013, 22 (3), pp.363 - 368. ⟨10.1038/ejhg.2013.135⟩. ⟨hal-01668667⟩
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