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Whole Exome Sequencing for the Diagnosis of Rare Genetic Neurodevelopmental Disorders Associated with Cerebellar Atrophy

Engy A. Ashaat,Hoda A. Ahmed,Nesma M. Elaraby,Alaaeldin Fayez,Ammal M. Metwally,Mona Mekkawy,Neveen A. Ashaat,Rasha Elhossini,Heba ElAwady,Randa Hesham Ali Abdelgawad,Mona El Gammal,Mohamed Ahmed Al Kersh,Dina Saleh

Research Square (Research Square)（2023）

引用 0|浏览11
关键词
disorders,diagnosis,genetic
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