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

Engy A. Ashaat,Hoda A. Ahmed,Nesma M. Elaraby,Alaaeldin Fayez,Ammal M. Metwally,Mona K. Mekkawy,Dalia Farouk Hussen,Neveen A. Ashaat,Rasha M. Elhossini, Heba Ahmed ElAwady,Randa H. A. Abdelgawad,Mona El Gammal,Mohamed Ahmed Al Kersh,Dina Amin Saleh

MOLECULAR NEUROBIOLOGY（2024）

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Key words
Neurodegenerative disorders,Neurological disorders,Novel variants,Cerebellar atrophy,WES
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