The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy
全外显子组测序在小脑萎缩相关罕见神经系统疾病谱系诊断中的价值
期刊:Molecular Neurobiology
影响因子:4.3
doi:10.1007/s12035-023-03866-y
Ashaat, Engy A; Ahmed, Hoda A; Elaraby, Nesma M; Fayez, Alaaeldin; Metwally, Ammal M; Mekkawy, Mona K; Hussen, Dalia Farouk; Ashaat, Neveen A; Elhossini, Rasha M; ElAwady, Heba Ahmed; Abdelgawad, Randa H A; Gammal, Mona El; Al Kersh, Mohamed Ahmed; Saleh, Dina Amin