TitleAuthorPublication DatePublisherType
    Novel mutation in an Egyptian patient with infantile Canavan disease.  Zaki, Osama K; El Abd, Heba S; Mohamed, Shaimaa A; Zayed, Hatem2016Springer Verlag (Germany)Article
    Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene  Moseilhy, Ahmed; Hassan, Magdy M.; El Abd, Heba S. A.; Mohammad, Shaimaa A.; El Bekay, Rajaa; Abdel-Motal, Ussama M.; Ouhtit, Allal; Zaki, Osama K.; Zayed, Hatem2016Springer USArticle
    Two patients with Canavan disease and structural modeling of a novel mutation.  Zaki, Osama K; Krishnamoorthy, Navaneethakrishnan; El Abd, Heba S; Harche, Soumaya A; Mattar, Reem A; Al Disi, Rana S; Nofal, Mariam Y; El Bekay, Rajaa; Ahmed, Khalid A; George Priya Doss, C; Zayed, Hatem2017Springer USArticle