Associated Papers
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder.
Yilmaz S et al.
Brain & Development, 2016
Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review.
Tanyalçin I et al.
European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society, 2013
Movement disorder and neuronal migration disorder due to ARFGEF2 mutation.
de Wit MC et al.
Neurogenetics, 2009
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