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You searched for: Author/Creator Vansenne, F.- Vansenne, F. [remove] 2
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- CDK13 -- congenital heart defects -- de novo variants -- developmental delay -- facial dysmorphism -- intellectual disability -- splice‐site variant -- whole‐exome sequencing 1
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- Early-onset ataxia -- Late-onset ataxia -- Dystonia -- Cortico-basal-ganglia-pontocerebellar pathway -- Nervous system development -- Disease continuum 1
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