All individuals with variants in gene WDR18

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00435631 Pat3 PubMed: Morleo 2023 2-generation family, 1 affected, unaffected non-carrier parents M no Pakistan - - - - - NDD see paper; ..., motor delay; no speech; intellectual disability; seizures; mild myopia; hypotonia; MRI brain abnormal white matter signal (hypomyelination); no; prominent maxilla/upper lip; micrognathia; long ears 1 1 Johan den Dunnen
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