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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.991721
Abstract: Introduction: Vici Syndrome is a rare, severe, neurodevelopmental/neurodegenerative disorder with multi-systemic manifestations presenting in infancy. It is mainly characterized by global developmental delay, seizures, agenesis of the corpus callosum, hair and skin hypopigmentation, bilateral cataract,…
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Keywords:
vici syndrome;
syndrome israel;
molecular insights;
clinical molecular ... See more keywords