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ArticleMolecular neurobiology2024

The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy.

Engy A Ashaat et al.PubMed ↗Full text ↗Publisher ↗

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4 papers cite it

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Full record →Abstract, authors, funding and every citing paper · PMID 38153683