All individuals with variants in gene AAR2

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00467801 Fam005PatBAB6682 PubMed: Charng 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents - yes Saudi Arabia - - - - - NDD developmental delay, microcephaly, cortical malformation, thin corpus callosum, ventricular septal defect, patent foramen ovale, anteriorly placed anus, skin macules 1 1 Johan den Dunnen
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