A Novel Heterozygous <i>De Novo MORC2</i> Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder

<div>Brain MRI in the patient at the age of 51 weeks. (a) Axial, T2-weighted images showing bilateral high signal intensity in the lentiform nuclei, putamen, and globus pallidus. (b) Axial, T2-weighted images showing bilateral high signal intensity in the cerebral peduncles and midbrain.</div>

Case Reports in Genetics

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Figure 2

Figure 2: A Novel Heterozygous <i>De Novo MORC2</i> Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder 

Case Reports in Genetics

A Novel Heterozygous De Novo MORC2 Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder

Figure 2