The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy.
Ashaat EA, Ahmed HA, Elaraby NM, Fayez A, Metwally AM, Mekkawy MK, Hussen DF, Ashaat NA, Elhossini RM, ElAwady HA, Abdelgawad RHA, Gammal ME, Al Kersh MA, Saleh DA.
Ashaat EA, et al. Among authors: ahmed ha.
Mol Neurobiol. 2023 Dec 28. doi: 10.1007/s12035-023-03866-y. Online ahead of print.
Mol Neurobiol. 2023.
PMID: 38153683