Irina Hüning

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In patients with genetically heterogeneous disorders such as intellectual disability or epilepsy, exome sequencing is a powerful tool to elucidate the underlying genetic cause. Homozygous and(More)
Approximately 2–5% of children are born with congenital abnormalities that manifest into more severe neurodevelopmental problems as they age.1 Neurodevelopmental disorders encompass a wide range of(More)
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