APA

Al Dhaibani M. A., El-Hattab A. W., Ismayl O. & Suleiman J. (20191010). B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss. : Neuropediatrics.

Chicago

Al Dhaibani Muna A, El-Hattab Ayman W, Ismayl Omar and Suleiman Jehan. 20191010. B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss. : Neuropediatrics.

Harvard

Al Dhaibani M. A., El-Hattab A. W., Ismayl O. and Suleiman J. (20191010). B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss. : Neuropediatrics.

MLA

Al Dhaibani Muna A, El-Hattab Ayman W, Ismayl Omar and Suleiman Jehan. B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss. : Neuropediatrics. 20191010.