All individuals with variants in gene INTS8

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00081355 FamINTS8Pat1/2/3 Mancini, NVHG2016, PubMed: Oegema 2017 2-generation family, 3 affected sibs (F, 2M), unaffected heterozygous carrier parents F;M - Netherlands - - - - - ID see paper; ..., epilepsy, microcephaly, cerebral blindness; MRI-brain periventricular nodular heterotopia (mostly frontal regions), cerebellar hypoplasia; broad nasal bridge, prominent glabella, hypertelorism, abnormal overlapping digits 2 3 Johan den Dunnen
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