All individuals with variants in gene FAM19A4

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00444499 Pat;Pat1 PubMed: Vuillaume 2018, PubMed: Riquin 2023 patient F - France - - - - - NDD see paper; ..., intellectual disability severe (IQ 20), global developmental delay, hypotonia, absent speech, autism; 7y-epilepsy; cerebral MRI: small periventricular heterotopia and dilated, cortical veins, extensive naevus; height -1.7 SD, weight +0.5 SD 1 1 Johan den Dunnen
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